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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_001288748.2 → NP_001275677.1 prolyl 4-hydroxylase subunit alpha-3 isoform 2 precursor
See identical proteins and their annotated locations for NP_001275677.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (2) uses an alternate splice site in the central coding region, which results in a frameshift, compared to variant 1. The encoded isoform (2) has a longer and distinct C-terminus, compared to isoform 1.
- Source sequence(s)
-
AK300598, HY188166
- Consensus CDS
-
CCDS73347.1
- UniProtKB/Swiss-Prot
-
Q7Z4N8
- Related
- ENSP00000401749.2, ENST00000427714.2
- Conserved Domains (3) summary
-
- smart00702
Location:356 → 478
- P4Hc; Prolyl 4-hydroxylase alpha subunit homologues
- pfam08336
Location:58 → 159
- P4Ha_N; Prolyl 4-Hydroxylase alpha-subunit, N-terminal region
- pfam13424
Location:186 → 252
- TPR_12; Tetratricopeptide repeat
-
NM_182904.5 → NP_878907.1 prolyl 4-hydroxylase subunit alpha-3 isoform 1 precursor
See identical proteins and their annotated locations for NP_878907.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (1) represents the longer transcript and encodes the shorter isoform (1).
- Source sequence(s)
-
AY358521, HY004548
- Consensus CDS
-
CCDS8230.1
- UniProtKB/Swiss-Prot
- A0AV13, B4DUD3, Q5EBL3, Q5JPA9, Q7Z4N8
- Related
- ENSP00000332170.4, ENST00000331597.9
- Conserved Domains (2) summary
-
- smart00702
Location:356 → 528
- P4Hc; Prolyl 4-hydroxylase alpha subunit homologues
- pfam08336
Location:58 → 159
- P4Ha_N; Prolyl 4-Hydroxylase alpha-subunit, N-terminal region
RNA
-
NR_110031.2 RNA Sequence
Status: REVIEWED
- Description
- Transcript Variant: This variant (3) lacks an internal exon and uses an alternate splice site at an internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AY358521, BC040582, HY004548
- Related
-
ENST00000525968.1