Canonical Allele Identifier: CA2008294941

Gene: KCNJ5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128916763T= , CM000673.2:g.128916763T=	GRCh38
NC_000011.9:g.128786658T= , CM000673.1:g.128786658T=	GRCh37
NC_000011.8:g.128291868T=	NCBI36
NG_023406.2:g.30346T= , LRG_333:g.30346T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.*32T= MANE Select	ENSP00000433295.1:n.*32T=
ENST00000338350.4:c.*32T=	ENSP00000339960.4:n.*32T=
ENST00000529694.5:c.*32T=	ENSP00000433295.1:n.*32T=
NM_000890.3:c.*32T= , LRG_333t1:c.*32T=	NP_000881.3:n.*32T=
XM_011542809.1:c.*32T=	XP_011541111.1:n.*32T=
XM_011542810.1:c.*32T=	XP_011541112.1:n.*32T=
NM_000890.4:c.*32T=	NP_000881.3:n.*32T=
NM_001354169.1:c.*32T=	NP_001341098.1:n.*32T=
XM_011542809.2:c.*32T=	XP_011541111.1:n.*32T=
XM_011542810.3:c.*32T=	XP_011541112.1:n.*32T=
NM_000890.5:c.*32T= MANE Select	NP_000881.3:n.*32T=
NM_001354169.2:c.*32T=	NP_001341098.1:n.*32T=