Canonical Allele Identifier: CA2008292640

Gene: KCNJ5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128911745A= , CM000673.2:g.128911745A=	GRCh38
NC_000011.9:g.128781640A= , CM000673.1:g.128781640A=	GRCh37
NC_000011.8:g.128286850A=	NCBI36
NG_023406.2:g.25328A= , LRG_333:g.25328A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000890.5:c.472A= MANE Select	NP_000881.3:p.Thr158=
ENST00000529694.6:c.472A= MANE Select	ENSP00000433295.1:p.Thr158=
NM_000890.3:c.472A= , LRG_333t1:c.472A=	NP_000881.3:p.Thr158=
NM_000890.4:c.472A=	NP_000881.3:p.Thr158=
NM_001354169.1:c.472A=	NP_001341098.1:p.Thr158=
NM_001354169.2:c.472A=	NP_001341098.1:p.Thr158=
ENST00000338350.4:c.472A=	ENSP00000339960.4:p.Thr158=
ENST00000529694.5:c.472A=	ENSP00000433295.1:p.Thr158=
ENST00000533599.1:c.472A=	ENSP00000434266.1:p.Thr158=
XM_011542809.1:c.472A=	XP_011541111.1:p.Thr158=
XM_011542809.2:c.472A=	XP_011541111.1:p.Thr158=
XM_011542810.1:c.472A=	XP_011541112.1:p.Thr158=
XM_011542810.3:c.472A=	XP_011541112.1:p.Thr158=