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These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome
annotation cycle, so their versions may not match the RefSeq versions in the current
genome build. Identify version mismatches by comparing the version of the RefSeq in
this section to the one reported in Genomic regions,
transcripts, and products above.
mRNA and Protein(s)
-
NM_001256666.2 → NP_001243595.1 protein FAM193A isoform 2
See identical proteins and their annotated locations for NP_001243595.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (2, also known as RES4-22B) includes an alternate exon in the 3' coding region, but maintains the reading frame, compared to variant 1. The encoded isoform (2) is longer than isoform 1.
- Source sequence(s)
-
AA905011, AB000460, BC136646
- Consensus CDS
-
CCDS58875.1
- UniProtKB/Swiss-Prot
- B7ZM85, B9EGR0, E9PFA1, O43607, P78311, P78312, P78313, Q9UEG8
- Related
- ENSP00000324587.5, ENST00000324666.9
- Conserved Domains (1) summary
-
- pfam15914
Location:1209 → 1262
- FAM193_C; FAM193 family C-terminal
-
NM_001256667.2 → NP_001243596.1 protein FAM193A isoform 3
Status: VALIDATED
- Description
- Transcript Variant: This variant (4) includes an alternate exon in the and uses an alternate splice site in the coding region, but maintains the reading frame, compared to variant 1. The encoded isoform (3) is longer than isoform 1.
- Source sequence(s)
-
AA905011, AB000459, BC144340
- Consensus CDS
-
CCDS58874.1
- UniProtKB/TrEMBL
-
E7EUR8
- Related
- ENSP00000427505.1, ENST00000502458.5
- Conserved Domains (1) summary
-
- pfam15914
Location:1190 → 1243
- FAM193_C; FAM193 family C-terminal
-
NM_001256668.2 → NP_001243597.1 protein FAM193A isoform 4
See identical proteins and their annotated locations for NP_001243597.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (5) includes an alternate exon in the 3' coding region, which results in a frameshift, compared to variant 1. The encoded isoform (4) is shorter and has a distinct C-terminus, compared to isoform 1.
- Source sequence(s)
-
AA905011, AB000459, BC144339, BM788933
- Consensus CDS
-
CCDS58876.1
- UniProtKB/TrEMBL
-
E7EUR8
- Related
- ENSP00000421200.1, ENST00000505311.5
- Conserved Domains (2) summary
-
- PRK12323
Location:661 → 738
- PRK12323; DNA polymerase III subunit gamma/tau
- pfam15914
Location:1168 → 1194
- FAM193_C; FAM193 family C-terminal
-
NM_001366316.2 → NP_001353245.1 protein FAM193A isoform 5
Status: VALIDATED
- Source sequence(s)
-
AL110117, BX322586, CR545473
- Conserved Domains (2) summary
-
- pfam15914
Location:1402 → 1455
- FAM193_C; FAM193 family C-terminal
- cl26386
Location:895 → 972
- DNA_pol3_gamma3; DNA polymerase III subunits gamma and tau domain III
-
NM_001366318.2 → NP_001353247.1 protein FAM193A isoform 6
Status: VALIDATED
- Description
- Transcript Variant: This variant (8) encodes the longest protein (isoform 6). This variant is inferred based on short read sequence data and conservation.
- Source sequence(s)
-
AL110117, BX322586, CR545473
- Consensus CDS
-
CCDS93467.1
- UniProtKB/TrEMBL
-
A0A1B0GVL4
- Related
- ENSP00000490564.1, ENST00000637812.2
- Conserved Domains (2) summary
-
- pfam15914
Location:1459 → 1512
- FAM193_C; FAM193 family C-terminal
- cl26386
Location:952 → 1029
- DNA_pol3_gamma3; DNA polymerase III subunits gamma and tau domain III
-
NM_003704.4 → NP_003695.3 protein FAM193A isoform 1
See identical proteins and their annotated locations for NP_003695.3
Status: VALIDATED
- Description
- Transcript Variant: This variant (1, also known as RES4-22A) encodes isoform 1.
- Source sequence(s)
-
AA905011, AB000459, AF040966, BM468825, D44687
- Consensus CDS
-
CCDS33943.1
- UniProtKB/TrEMBL
-
E7EUR8
- Related
- ENSP00000372290.3, ENST00000382839.7
- Conserved Domains (1) summary
-
- pfam15914
Location:1168 → 1221
- FAM193_C; FAM193 family C-terminal
RNA
-
NR_046335.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (3, also known as RES4-22C) uses an alternate splice site, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AA905011, AB000461, AF040966
- Related
-
ENST00000512465.5
-
NR_046336.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (6) contains an alternate exon and uses an alternate splice site in the 3' region, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AA905011, AB000459, AB000461, BC144337, BF924432, BM788933
- Related
-
ENST00000513898.5