Canonical Allele Identifier: CA2008293186

Gene: KCNJ5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128912070A= , CM000673.2:g.128912070A=	GRCh38
NC_000011.9:g.128781965A= , CM000673.1:g.128781965A=	GRCh37
NC_000011.8:g.128287175A=	NCBI36
NG_023406.2:g.25653A= , LRG_333:g.25653A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.797A= MANE Select	ENSP00000433295.1:p.Asp266=
ENST00000338350.4:c.797A=	ENSP00000339960.4:p.Asp266=
ENST00000529694.5:c.797A=	ENSP00000433295.1:p.Asp266=
ENST00000533599.1:c.797A=	ENSP00000434266.1:p.Asp266=
NM_000890.3:c.797A= , LRG_333t1:c.797A=	NP_000881.3:p.Asp266=
XM_011542809.1:c.797A=	XP_011541111.1:p.Asp266=
XM_011542810.1:c.797A=	XP_011541112.1:p.Asp266=
NM_000890.4:c.797A=	NP_000881.3:p.Asp266=
NM_001354169.1:c.797A=	NP_001341098.1:p.Asp266=
XM_011542809.2:c.797A=	XP_011541111.1:p.Asp266=
XM_011542810.3:c.797A=	XP_011541112.1:p.Asp266=
NM_000890.5:c.797A= MANE Select	NP_000881.3:p.Asp266=
NM_001354169.2:c.797A=	NP_001341098.1:p.Asp266=