Canonical Allele Identifier: CA2008283051

Gene: KCNJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128865375A= , CM000673.2:g.128865375A=	GRCh38
NC_000011.9:g.128735270A= , CM000673.1:g.128735270A=	GRCh37
NC_000011.8:g.128240480A=	NCBI36
NG_009379.1:g.6999T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.-192+1798T= MANE Select	ENSP00000376434.1:n.-192+1798T=
ENST00000324003.3:c.-192+1798T=	ENSP00000316136.3:n.-192+1798T=
ENST00000324036.7:c.-192+1148T=	ENSP00000316233.3:n.-192+1148T=
ENST00000392665.6:c.-22+1798T=	ENSP00000376433.2:n.-22+1798T=
ENST00000392666.5:c.-192+1798T=	ENSP00000376434.1:n.-192+1798T=
ENST00000440599.6:c.-22+1148T=	ENSP00000406320.2:n.-22+1148T=
ENST00000531562.1:n.124+1798T=
NM_153764.2:c.-22+1798T=	NP_722448.1:n.-22+1798T=
NM_153765.2:c.30+1148T=	NP_722449.3:n.30+1148T=
NM_153766.2:c.-192+1798T=	NP_722450.1:n.-192+1798T=
NM_153767.3:c.-192+1148T=	NP_722451.1:n.-192+1148T=
XR_001748442.1:n.3532+1365A=
NM_153764.3:c.-22+1798T=	NP_722448.1:n.-22+1798T=
NM_153765.3:c.30+1148T=	NP_722449.3:n.30+1148T=
NM_153766.3:c.-192+1798T= MANE Select	NP_722450.1:n.-192+1798T=
NM_153767.4:c.-192+1148T=	NP_722451.1:n.-192+1148T=