Human (GRCh38.p14)
Description

chromosome 17 open reading frame 100 [Source:HGNC Symbol;Acc:HGNC:34494]

Gene Synonyms

LOC388327

Location
About this transcript

This transcript has 1 exon, is annotated with 7 domains and features, is associated with 838 variant alleles and maps to 234 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000542475.3C17orf100-2011715118aaENSP00000491070.1
 
Protein coding
CCDS73952A8MU93 NM_001105520.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:NA
ENST00000635042.1C17orf100-2031062118aaENSP00000491523.1
 
Nonsense mediated decay
CCDS73952A8MU93 -TSL:5
ENST00000634977.1C17orf100-20281135aaENSP00000491769.1
 
Nonsense mediated decay
A0A1W2PPW6 -TSL:5CDS 5' incomplete
Statistics

Exons: 1, Coding exons: 1, Transcript length: 1,715 bps, Translation length: 118 residues

MANE

This MANE Select transcript contains ENSP00000491070 and matches to NM_001105520.2 and NP_001098990.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: A8MU93

CCDS

This transcript is a member of the Human CCDS set: CCDS73952

Transcript Support Level (TSL)

TSL:NA

Version

ENST00000542475.3

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

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