Canonical Allele Identifier: CA2008286203

Gene: KCNJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128839242_128839243delinsAG , CM000673.2:g.128839242_128839243delinsAG	GRCh38
NC_000011.9:g.128709137_128709138delinsAG , CM000673.1:g.128709137_128709138delinsAG	GRCh37
NC_000011.8:g.128214347_128214348delinsAG	NCBI36
NG_009379.1:g.33131_33132delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000392666.6:c.1001_1002delinsCT MANE Select	ENSP00000376434.1:p.Pro334=
ENST00000324036.7:c.1001_1002delinsCT	ENSP00000316233.3:p.Pro334=
ENST00000392664.2:c.1058_1059delinsCT	ENSP00000376432.2:p.Pro353=
ENST00000392665.6:c.1001_1002delinsCT	ENSP00000376433.2:p.Pro334=
ENST00000392666.5:c.1001_1002delinsCT	ENSP00000376434.1:p.Pro334=
ENST00000440599.6:c.1001_1002delinsCT	ENSP00000406320.2:p.Pro334=
NM_000220.4:c.1058_1059delinsCT	NP_000211.1:p.Pro353=
NM_153764.2:c.1001_1002delinsCT	NP_722448.1:p.Pro334=
NM_153765.2:c.1052_1053delinsCT	NP_722449.3:p.Pro351=
NM_153766.2:c.1001_1002delinsCT	NP_722450.1:p.Pro334=
NM_153767.3:c.1001_1002delinsCT	NP_722451.1:p.Pro334=
NM_000220.6:c.1058_1059delinsCT	NP_000211.1:p.Pro353=
NM_153764.3:c.1001_1002delinsCT	NP_722448.1:p.Pro334=
NM_153765.3:c.1052_1053delinsCT	NP_722449.3:p.Pro351=
NM_153766.3:c.1001_1002delinsCT MANE Select	NP_722450.1:p.Pro334=
NM_153767.4:c.1001_1002delinsCT	NP_722451.1:p.Pro334=