Canonical Allele Identifier: CA2008286733

Gene: KCNJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128839595T= , CM000673.2:g.128839595T=	GRCh38
NC_000011.9:g.128709490T= , CM000673.1:g.128709490T=	GRCh37
NC_000011.8:g.128214700T=	NCBI36
NG_009379.1:g.32779A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.649A= MANE Select	ENSP00000376434.1:p.Thr217=
ENST00000324036.7:c.649A=	ENSP00000316233.3:p.Thr217=
ENST00000392664.2:c.706A=	ENSP00000376432.2:p.Thr236=
ENST00000392665.6:c.649A=	ENSP00000376433.2:p.Thr217=
ENST00000392666.5:c.649A=	ENSP00000376434.1:p.Thr217=
ENST00000440599.6:c.649A=	ENSP00000406320.2:p.Thr217=
NM_000220.4:c.706A=	NP_000211.1:p.Thr236=
NM_153764.2:c.649A=	NP_722448.1:p.Thr217=
NM_153765.2:c.700A=	NP_722449.3:p.Thr234=
NM_153766.2:c.649A=	NP_722450.1:p.Thr217=
NM_153767.3:c.649A=	NP_722451.1:p.Thr217=
NM_000220.6:c.706A=	NP_000211.1:p.Thr236=
NM_153764.3:c.649A=	NP_722448.1:p.Thr217=
NM_153765.3:c.700A=	NP_722449.3:p.Thr234=
NM_153766.3:c.649A= MANE Select	NP_722450.1:p.Thr217=
NM_153767.4:c.649A=	NP_722451.1:p.Thr217=