Human (GRCh38.p14)
Description

signal recognition particle 9 [Source:HGNC Symbol;Acc:HGNC:11304]

Location

Chromosome 1: 225,777,813-225,790,468 forward strand.

GRCh38:CM000663.2

About this gene

This gene has 9 transcripts (splice variants) and 208 orthologues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000304786.12SRP9-201148186aaENSP00000305230.7
 
Protein coding
CCDS1546P49458-1 NM_003133.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000366839.8SRP9-203159682aaENSP00000355804.4
 
Protein coding
CCDS44323P49458-2 -GENCODE basicTSL:1
ENST00000651761.1SRP9-209142052aaENSP00000498520.1
 
Protein coding
Q659G3 -GENCODE basic
ENST00000650651.1SRP9-20654849aaENSP00000498987.1
 
Protein coding
Q6P2S0 -GENCODE basic
ENST00000366838.1SRP9-20254066aaENSP00000355803.1
 
Protein coding
E9PE20 -GENCODE basicTSL:2
ENST00000619790.4SRP9-20437782aaENSP00000485002.1
 
Protein coding
CCDS44323P49458-2 -GENCODE basicTSL:2
ENST00000626563.2SRP9-20532966aaENSP00000485985.1
 
Protein coding
E9PE20 -GENCODE basicTSL:5
ENST00000651465.1SRP9-20785682aaENSP00000498359.1
 
Nonsense mediated decay
CCDS44323P49458-2 --
ENST00000651653.1SRP9-208522No protein-
 
Retained intron
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