Canonical Allele Identifier: CA2008283131

Gene: KCNJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128865532A= , CM000673.2:g.128865532A=	GRCh38
NC_000011.9:g.128735427A= , CM000673.1:g.128735427A=	GRCh37
NC_000011.8:g.128240637A=	NCBI36
NG_009379.1:g.6842T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.-192+1641T= MANE Select	ENSP00000376434.1:n.-192+1641T=
ENST00000324003.3:c.-192+1641T=	ENSP00000316136.3:n.-192+1641T=
ENST00000324036.7:c.-192+991T=	ENSP00000316233.3:n.-192+991T=
ENST00000392665.6:c.-22+1641T=	ENSP00000376433.2:n.-22+1641T=
ENST00000392666.5:c.-192+1641T=	ENSP00000376434.1:n.-192+1641T=
ENST00000440599.6:c.-22+991T=	ENSP00000406320.2:n.-22+991T=
ENST00000531562.1:n.124+1641T=
NM_153764.2:c.-22+1641T=	NP_722448.1:n.-22+1641T=
NM_153765.2:c.30+991T=	NP_722449.3:n.30+991T=
NM_153766.2:c.-192+1641T=	NP_722450.1:n.-192+1641T=
NM_153767.3:c.-192+991T=	NP_722451.1:n.-192+991T=
XR_001748442.1:n.3533-1218A=
NM_153764.3:c.-22+1641T=	NP_722448.1:n.-22+1641T=
NM_153765.3:c.30+991T=	NP_722449.3:n.30+991T=
NM_153766.3:c.-192+1641T= MANE Select	NP_722450.1:n.-192+1641T=
NM_153767.4:c.-192+991T=	NP_722451.1:n.-192+991T=