Canonical Allele Identifier: CA2008251487

Gene: KCNJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128839982T= , CM000673.2:g.128839982T=	GRCh38
NC_000011.9:g.128709877T= , CM000673.1:g.128709877T=	GRCh37
NC_000011.8:g.128215087T=	NCBI36
NG_009379.1:g.32392A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.262A= MANE Select	ENSP00000376434.1:p.Lys88=
ENST00000324003.3:c.262A=	ENSP00000316136.3:p.Lys88=
ENST00000324036.7:c.262A=	ENSP00000316233.3:p.Lys88=
ENST00000392664.2:c.319A=	ENSP00000376432.2:p.Lys107=
ENST00000392665.6:c.262A=	ENSP00000376433.2:p.Lys88=
ENST00000392666.5:c.262A=	ENSP00000376434.1:p.Lys88=
ENST00000440599.6:c.262A=	ENSP00000406320.2:p.Lys88=
NM_000220.4:c.319A=	NP_000211.1:p.Lys107=
NM_153764.2:c.262A=	NP_722448.1:p.Lys88=
NM_153765.2:c.313A=	NP_722449.3:p.Lys105=
NM_153766.2:c.262A=	NP_722450.1:p.Lys88=
NM_153767.3:c.262A=	NP_722451.1:p.Lys88=
NM_000220.6:c.319A=	NP_000211.1:p.Lys107=
NM_153764.3:c.262A=	NP_722448.1:p.Lys88=
NM_153765.3:c.313A=	NP_722449.3:p.Lys105=
NM_153766.3:c.262A= MANE Select	NP_722450.1:p.Lys88=
NM_153767.4:c.262A=	NP_722451.1:p.Lys88=