Human (GRCh38.p14)
Description

CFAP97 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:37241]

Gene Synonyms

C17ORF105

Location
About this transcript

This transcript has 6 exons, is annotated with 4 domains and features, is associated with 2764 variant alleles and maps to 280 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000449302.8CFAP97D1-2013761164aaENSP00000415662.2
 
Protein coding
CCDS45695B2RV13 NM_001136483.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000590148.1CFAP97D1-20252058aaENSP00000468141.1
 
Nonsense mediated decay
K7ER76 -TSL:4CDS 5' incomplete
Statistics

Exons: 6, Coding exons: 5, Transcript length: 3,761 bps, Translation length: 164 residues

MANE

This MANE Select transcript contains ENSP00000415662 and matches to NM_001136483.3 and NP_001129955.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: B2RV13

CCDS

This transcript is a member of the Human CCDS set: CCDS45695

Transcript Support Level (TSL)

TSL:1

Version

ENST00000449302.8

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.