Human (GRCh38.p14)
Description

STIM activating enhancer [Source:HGNC Symbol;Acc:HGNC:30526]

Gene Synonyms

MGC52022, TMEM110

Location
About this transcript

This transcript has 8 exons, is annotated with 12 domains and features, is associated with 25844 variant alleles and maps to 827 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000355083.11STIMATE-2014744294aaENSP00000347195.5
 
Protein coding
CCDS2866Q86TL2 NM_198563.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000482155.1STIMATE-20552539aaENSP00000418967.1
 
Protein coding
H7C551 -TSL:4CDS 5' incomplete
ENST00000485356.1STIMATE-20651489aaENSP00000418652.1
 
Protein coding
H7C503 -TSL:2CDS 5' incomplete
ENST00000467979.1STIMATE-20345865aaENSP00000420219.1
 
Nonsense mediated decay
F8WDI5 -TSL:3
ENST00000464769.1STIMATE-202542No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000477591.1STIMATE-204488No protein-
 
Protein coding CDS not defined
--TSL:1
Statistics

Exons: 8, Coding exons: 8, Transcript length: 4,744 bps, Translation length: 294 residues

MANE

This MANE Select transcript contains ENSP00000347195 and matches to NM_198563.5 and NP_940965.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q86TL2

CCDS

This transcript is a member of the Human CCDS set: CCDS2866

Transcript Support Level (TSL)

TSL:1

Version

ENST00000355083.11

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.