Canonical Allele Identifier: CA2008255161

Gene: KCNJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128842886G= , CM000673.2:g.128842886G=	GRCh38
NC_000011.9:g.128712781G= , CM000673.1:g.128712781G=	GRCh37
NC_000011.8:g.128217991G=	NCBI36
NG_009379.1:g.29488C=

Transcript Alleles

HGVS	Amino-acid Change
NM_153766.3:c.-21-2622C= MANE Select	NP_722450.1:n.-21-2622C=
ENST00000392666.6:c.-21-2622C= MANE Select	ENSP00000376434.1:n.-21-2622C=
NM_153764.2:c.-21-2622C=	NP_722448.1:n.-21-2622C=
NM_153764.3:c.-21-2622C=	NP_722448.1:n.-21-2622C=
NM_153765.2:c.31-2622C=	NP_722449.3:n.31-2622C=
NM_153765.3:c.31-2622C=	NP_722449.3:n.31-2622C=
NM_153766.2:c.-21-2622C=	NP_722450.1:n.-21-2622C=
NM_153767.3:c.-21-2622C=	NP_722451.1:n.-21-2622C=
NM_153767.4:c.-21-2622C=	NP_722451.1:n.-21-2622C=
ENST00000324003.3:c.-21-2622C=	ENSP00000316136.3:n.-21-2622C=
ENST00000324036.7:c.-21-2622C=	ENSP00000316233.3:n.-21-2622C=
ENST00000392665.6:c.-21-2622C=	ENSP00000376433.2:n.-21-2622C=
ENST00000392666.5:c.-21-2622C=	ENSP00000376434.1:n.-21-2622C=
ENST00000440599.6:c.-21-2622C=	ENSP00000406320.2:n.-21-2622C=
ENST00000531562.1:n.325-2622C=