Canonical Allele Identifier: CA477703129

Gene: KCNJ1

Linked Data

• MyVariant Identifiers: chr11:g.128709440T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128839545T>G , CM000673.2:g.128839545T>G	GRCh38
NC_000011.9:g.128709440T>G , CM000673.1:g.128709440T>G	GRCh37
NC_000011.8:g.128214650T>G	NCBI36
NG_009379.1:g.32829A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000392666.6:c.699A>C MANE Select	ENSP00000376434.1:p.Val233=
ENST00000324036.7:c.699A>C	ENSP00000316233.3:p.Val233=
ENST00000392664.2:c.756A>C	ENSP00000376432.2:p.Val252=
ENST00000392665.6:c.699A>C	ENSP00000376433.2:p.Val233=
ENST00000392666.5:c.699A>C	ENSP00000376434.1:p.Val233=
ENST00000440599.6:c.699A>C	ENSP00000406320.2:p.Val233=
NM_000220.4:c.756A>C	NP_000211.1:p.Val252=
NM_153764.2:c.699A>C	NP_722448.1:p.Val233=
NM_153765.2:c.750A>C	NP_722449.3:p.Val250=
NM_153766.2:c.699A>C	NP_722450.1:p.Val233=
NM_153767.3:c.699A>C	NP_722451.1:p.Val233=
NM_000220.6:c.756A>C	NP_000211.1:p.Val252=
NM_153764.3:c.699A>C	NP_722448.1:p.Val233=
NM_153765.3:c.750A>C	NP_722449.3:p.Val250=
NM_153766.3:c.699A>C MANE Select	NP_722450.1:p.Val233=
NM_153767.4:c.699A>C	NP_722451.1:p.Val233=