Canonical Allele Identifier: CA2008250977

Gene: KCNJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128839739G= , CM000673.2:g.128839739G=	GRCh38
NC_000011.9:g.128709634G= , CM000673.1:g.128709634G=	GRCh37
NC_000011.8:g.128214844G=	NCBI36
NG_009379.1:g.32635C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.505C= MANE Select	ENSP00000376434.1:p.Arg169=
ENST00000324036.7:c.505C=	ENSP00000316233.3:p.Arg169=
ENST00000392664.2:c.562C=	ENSP00000376432.2:p.Arg188=
ENST00000392665.6:c.505C=	ENSP00000376433.2:p.Arg169=
ENST00000392666.5:c.505C=	ENSP00000376434.1:p.Arg169=
ENST00000440599.6:c.505C=	ENSP00000406320.2:p.Arg169=
NM_000220.4:c.562C=	NP_000211.1:p.Arg188=
NM_153764.2:c.505C=	NP_722448.1:p.Arg169=
NM_153765.2:c.556C=	NP_722449.3:p.Arg186=
NM_153766.2:c.505C=	NP_722450.1:p.Arg169=
NM_153767.3:c.505C=	NP_722451.1:p.Arg169=
NM_000220.6:c.562C=	NP_000211.1:p.Arg188=
NM_153764.3:c.505C=	NP_722448.1:p.Arg169=
NM_153765.3:c.556C=	NP_722449.3:p.Arg186=
NM_153766.3:c.505C= MANE Select	NP_722450.1:p.Arg169=
NM_153767.4:c.505C=	NP_722451.1:p.Arg169=