Human (GRCh38.p14)
Description

signal recognition particle 19 [Source:HGNC Symbol;Acc:HGNC:11300]

Location

Chromosome 5: 112,861,188-112,898,371 forward strand.

GRCh38:CM000667.2

About this gene

This gene has 12 transcripts (splice variants), 209 orthologues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000505459.6SRP19-2062776144aaENSP00000424870.1
 
Protein coding
CCDS4108P09132-1 NM_003135.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000391338.3SRP19-2021850101aaENSP00000375133.2
 
Protein coding
CCDS87319A0A2U3TZN1 -GENCODE basicTSL:NA
ENST00000621420.5SRP19-2121270120aaENSP00000482018.1
 
Protein coding
CCDS75286A0A087WYR0 -GENCODE basicTSL:3
ENST00000282999.7SRP19-201937110aaENSP00000282999.3
 
Protein coding
CCDS56375P09132-2 -GENCODE basicTSL:1
ENST00000445150.3SRP19-203833104aaENSP00000480521.1
 
Protein coding
A0A087WWU9 -GENCODE basicTSL:2
ENST00000515463.1SRP19-21066078aaENSP00000425562.1
 
Protein coding
CCDS56376P09132-3 -GENCODE basicTSL:3
ENST00000503445.5SRP19-20450677aaENSP00000493920.1
 
Protein coding
A0A2R8Y4M3 -GENCODE basicTSL:3
ENST00000506997.2SRP19-208706343aaENSP00000424153.1
 
Nonsense mediated decay
D6RBG4 -TSL:3
ENST00000506987.1SRP19-207727No protein-
 
Retained intron
--TSL:2
ENST00000515755.1SRP19-211631No protein-
 
Retained intron
--TSL:2
ENST00000509024.2SRP19-209474No protein-
 
Retained intron
--TSL:2
ENST00000504696.1SRP19-205473No protein-
 
Retained intron
--TSL:2