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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_030945.4 → NP_112207.1 complement C1q tumor necrosis factor-related protein 3 isoform a precursor
See identical proteins and their annotated locations for NP_112207.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) represents the shortest transcript and encodes the shorter isoform (a).
- Source sequence(s)
-
AC139783, AF329837, AK295968, BX640995
- Consensus CDS
-
CCDS3904.1
- UniProtKB/Swiss-Prot
- Q0VAN4, Q542Y2, Q6MZN1, Q96KY1, Q9BXJ4
- Related
- ENSP00000231338.7, ENST00000231338.7
- Conserved Domains (2) summary
-
- pfam01391
Location:71 → 113
- Collagen; Collagen triple helix repeat (20 copies)
- pfam00386
Location:119 → 242
- C1q; C1q domain
-
NM_181435.6 → NP_852100.3 complement C1q tumor necrosis factor-related protein 3 isoform b precursor
See identical proteins and their annotated locations for NP_852100.3
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) uses an alternate in-frame splice site that results in an additional segment in the 5' coding region, compared to variant 1. The encoded isoform (b) is longer than isoform a.
- Source sequence(s)
-
AC139783, AK295968, BX640995
- Consensus CDS
-
CCDS34141.1
- UniProtKB/Swiss-Prot
-
Q9BXJ4
- Related
- ENSP00000371497.3, ENST00000382065.8
- Conserved Domains (2) summary
-
- pfam01391
Location:144 → 186
- Collagen; Collagen triple helix repeat (20 copies)
- pfam00386
Location:192 → 315
- C1q; C1q domain
RNA
-
NR_146599.1 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (3) uses a different 5' exon structure compared to variant 1. This variant is represented as non-coding because it lacks a large portion of the coding region, including the translational start codon, found in variant 1.
- Source sequence(s)
-
AC138409, AC139783, AC139792
The following sections contain reference sequences that belong to a
specific genome build. Explain
This section includes genomic Reference
Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as
RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate
assemblies. Model RNAs and proteins are also reported here.
Reference GRCh38.p14 Primary Assembly
Genomic
-
NC_000005.10 Reference GRCh38.p14 Primary Assembly
- Range
-
34017858..34244724 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060929.1 Alternate T2T-CHM13v2.0
- Range
-
34139780..34489333 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)