Canonical Allele Identifier: CA6358019
Gene: KCNJ5 HGNC NCBI

Linked Data

ClinVar Variation Id: 457004
dbSNP Id: rs780934792

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128916661A>G , CM000673.2:g.128916661A>G GRCh38
NC_000011.9:g.128786556A>G , CM000673.1:g.128786556A>G GRCh37
NC_000011.8:g.128291766A>G NCBI36
NG_023406.2:g.30244A>G , LRG_333:g.30244A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000529694.6:c.1190A>G MANE Select ENSP00000433295.1:p.Glu397Gly
ENST00000338350.4:c.1190A>G ENSP00000339960.4:p.Glu397Gly
ENST00000529694.5:c.1190A>G ENSP00000433295.1:p.Glu397Gly
ENST00000533599.1:c.1190A>G ENSP00000434266.1:p.Glu397Gly
NM_000890.3:c.1190A>G , LRG_333t1:c.1190A>G NP_000881.3:p.Glu397Gly
XM_011542809.1:c.1190A>G XP_011541111.1:p.Glu397Gly
XM_011542810.1:c.1190A>G XP_011541112.1:p.Glu397Gly
NM_000890.4:c.1190A>G NP_000881.3:p.Glu397Gly
NM_001354169.1:c.1190A>G NP_001341098.1:p.Glu397Gly
XM_011542809.2:c.1190A>G XP_011541111.1:p.Glu397Gly
XM_011542810.3:c.1190A>G XP_011541112.1:p.Glu397Gly
NM_000890.5:c.1190A>G MANE Select NP_000881.3:p.Glu397Gly
NM_001354169.2:c.1190A>G NP_001341098.1:p.Glu397Gly