Canonical Allele Identifier: CA2008294886

Gene: KCNJ5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128916640C= , CM000673.2:g.128916640C=	GRCh38
NC_000011.9:g.128786535C= , CM000673.1:g.128786535C=	GRCh37
NC_000011.8:g.128291745C=	NCBI36
NG_023406.2:g.30223C= , LRG_333:g.30223C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529694.6:c.1169C= MANE Select	ENSP00000433295.1:p.Ala390=
ENST00000338350.4:c.1169C=	ENSP00000339960.4:p.Ala390=
ENST00000529694.5:c.1169C=	ENSP00000433295.1:p.Ala390=
ENST00000533599.1:c.1169C=	ENSP00000434266.1:p.Ala390=
NM_000890.3:c.1169C= , LRG_333t1:c.1169C=	NP_000881.3:p.Ala390=
XM_011542809.1:c.1169C=	XP_011541111.1:p.Ala390=
XM_011542810.1:c.1169C=	XP_011541112.1:p.Ala390=
NM_000890.4:c.1169C=	NP_000881.3:p.Ala390=
NM_001354169.1:c.1169C=	NP_001341098.1:p.Ala390=
XM_011542809.2:c.1169C=	XP_011541111.1:p.Ala390=
XM_011542810.3:c.1169C=	XP_011541112.1:p.Ala390=
NM_000890.5:c.1169C= MANE Select	NP_000881.3:p.Ala390=
NM_001354169.2:c.1169C=	NP_001341098.1:p.Ala390=