Canonical Allele Identifier: CA383244930

Gene: KCNJ1

Linked Data

• MyVariant Identifiers: chr11:g.128709663A>G (hg19) ; chr11:g.128839768A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128839768A>G , CM000673.2:g.128839768A>G	GRCh38
NC_000011.9:g.128709663A>G , CM000673.1:g.128709663A>G	GRCh37
NC_000011.8:g.128214873A>G	NCBI36
NG_009379.1:g.32606T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.476T>C MANE Select	ENSP00000376434.1:p.Ile159Thr
ENST00000324036.7:c.476T>C	ENSP00000316233.3:p.Ile159Thr
ENST00000392664.2:c.533T>C	ENSP00000376432.2:p.Ile178Thr
ENST00000392665.6:c.476T>C	ENSP00000376433.2:p.Ile159Thr
ENST00000392666.5:c.476T>C	ENSP00000376434.1:p.Ile159Thr
ENST00000440599.6:c.476T>C	ENSP00000406320.2:p.Ile159Thr
NM_000220.4:c.533T>C	NP_000211.1:p.Ile178Thr
NM_153764.2:c.476T>C	NP_722448.1:p.Ile159Thr
NM_153765.2:c.527T>C	NP_722449.3:p.Ile176Thr
NM_153766.2:c.476T>C	NP_722450.1:p.Ile159Thr
NM_153767.3:c.476T>C	NP_722451.1:p.Ile159Thr
NM_000220.6:c.533T>C	NP_000211.1:p.Ile178Thr
NM_153764.3:c.476T>C	NP_722448.1:p.Ile159Thr
NM_153765.3:c.527T>C	NP_722449.3:p.Ile176Thr
NM_153766.3:c.476T>C MANE Select	NP_722450.1:p.Ile159Thr
NM_153767.4:c.476T>C	NP_722451.1:p.Ile159Thr