Human (GRCh38.p14)
Description

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

Location
About this transcript

This transcript has 7 exons, is associated with 11757 variant alleles and maps to 349 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

Protein domains for ENSP00000463396.1