Human (GRCh38.p14)
Description

SNRPN upstream open reading frame [Source:HGNC Symbol;Acc:HGNC:11171]

Location
About this transcript

This transcript has 3 exons, is annotated with 3 domains and features, is associated with 7346 variant alleles and maps to 241 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000577949.6SNURF-202106271aaENSP00000463201.1
 
Protein coding
CCDS10016A0A024R0T6 Q9Y675 NM_001394334.1MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:2
ENST00000338327.4SNURF-20133171aaENSP00000342152.4
 
Protein coding
CCDS10016A0A024R0T6 Q9Y675 -GENCODE basicAPPRIS P1TSL:5
ENST00000580062.5SNURF-20379671aaENSP00000463396.1
 
Nonsense mediated decay
CCDS10016A0A024R0T6 Q9Y675 -TSL:3
Statistics

Exons: 3, Coding exons: 3, Transcript length: 1,062 bps, Translation length: 71 residues

MANE

This MANE Select transcript contains ENSP00000463201 and matches to NM_001394334.1 and NP_001381263.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9Y675

CCDS

This transcript is a member of the Human CCDS set: CCDS10016

Transcript Support Level (TSL)

TSL:2

Version

ENST00000577949.6

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.