Canonical Allele Identifier: CA477703282

Gene: KCNJ1

Linked Data

• MyVariant Identifiers: chr11:g.128709563G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128839668G>T , CM000673.2:g.128839668G>T	GRCh38
NC_000011.9:g.128709563G>T , CM000673.1:g.128709563G>T	GRCh37
NC_000011.8:g.128214773G>T	NCBI36
NG_009379.1:g.32706C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.576C>A MANE Select	ENSP00000376434.1:p.Ile192=
ENST00000324036.7:c.576C>A	ENSP00000316233.3:p.Ile192=
ENST00000392664.2:c.633C>A	ENSP00000376432.2:p.Ile211=
ENST00000392665.6:c.576C>A	ENSP00000376433.2:p.Ile192=
ENST00000392666.5:c.576C>A	ENSP00000376434.1:p.Ile192=
ENST00000440599.6:c.576C>A	ENSP00000406320.2:p.Ile192=
NM_000220.4:c.633C>A	NP_000211.1:p.Ile211=
NM_153764.2:c.576C>A	NP_722448.1:p.Ile192=
NM_153765.2:c.627C>A	NP_722449.3:p.Ile209=
NM_153766.2:c.576C>A	NP_722450.1:p.Ile192=
NM_153767.3:c.576C>A	NP_722451.1:p.Ile192=
NM_000220.6:c.633C>A	NP_000211.1:p.Ile211=
NM_153764.3:c.576C>A	NP_722448.1:p.Ile192=
NM_153765.3:c.627C>A	NP_722449.3:p.Ile209=
NM_153766.3:c.576C>A MANE Select	NP_722450.1:p.Ile192=
NM_153767.4:c.576C>A	NP_722451.1:p.Ile192=