Canonical Allele Identifier: CA2008286626

Gene: KCNJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128839514T= , CM000673.2:g.128839514T=	GRCh38
NC_000011.9:g.128709409T= , CM000673.1:g.128709409T=	GRCh37
NC_000011.8:g.128214619T=	NCBI36
NG_009379.1:g.32860A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.730A= MANE Select	ENSP00000376434.1:p.Ile244=
ENST00000324036.7:c.730A=	ENSP00000316233.3:p.Ile244=
ENST00000392664.2:c.787A=	ENSP00000376432.2:p.Ile263=
ENST00000392665.6:c.730A=	ENSP00000376433.2:p.Ile244=
ENST00000392666.5:c.730A=	ENSP00000376434.1:p.Ile244=
ENST00000440599.6:c.730A=	ENSP00000406320.2:p.Ile244=
NM_000220.4:c.787A=	NP_000211.1:p.Ile263=
NM_153764.2:c.730A=	NP_722448.1:p.Ile244=
NM_153765.2:c.781A=	NP_722449.3:p.Ile261=
NM_153766.2:c.730A=	NP_722450.1:p.Ile244=
NM_153767.3:c.730A=	NP_722451.1:p.Ile244=
NM_000220.6:c.787A=	NP_000211.1:p.Ile263=
NM_153764.3:c.730A=	NP_722448.1:p.Ile244=
NM_153765.3:c.781A=	NP_722449.3:p.Ile261=
NM_153766.3:c.730A= MANE Select	NP_722450.1:p.Ile244=
NM_153767.4:c.730A=	NP_722451.1:p.Ile244=