Canonical Allele Identifier: CA477703222

Gene: KCNJ1

Linked Data

• MyVariant Identifiers: chr11:g.128709494T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128839599T>C , CM000673.2:g.128839599T>C	GRCh38
NC_000011.9:g.128709494T>C , CM000673.1:g.128709494T>C	GRCh37
NC_000011.8:g.128214704T>C	NCBI36
NG_009379.1:g.32775A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.645A>G MANE Select	ENSP00000376434.1:p.Thr215=
ENST00000324036.7:c.645A>G	ENSP00000316233.3:p.Thr215=
ENST00000392664.2:c.702A>G	ENSP00000376432.2:p.Thr234=
ENST00000392665.6:c.645A>G	ENSP00000376433.2:p.Thr215=
ENST00000392666.5:c.645A>G	ENSP00000376434.1:p.Thr215=
ENST00000440599.6:c.645A>G	ENSP00000406320.2:p.Thr215=
NM_000220.4:c.702A>G	NP_000211.1:p.Thr234=
NM_153764.2:c.645A>G	NP_722448.1:p.Thr215=
NM_153765.2:c.696A>G	NP_722449.3:p.Thr232=
NM_153766.2:c.645A>G	NP_722450.1:p.Thr215=
NM_153767.3:c.645A>G	NP_722451.1:p.Thr215=
NM_000220.6:c.702A>G	NP_000211.1:p.Thr234=
NM_153764.3:c.645A>G	NP_722448.1:p.Thr215=
NM_153765.3:c.696A>G	NP_722449.3:p.Thr232=
NM_153766.3:c.645A>G MANE Select	NP_722450.1:p.Thr215=
NM_153767.4:c.645A>G	NP_722451.1:p.Thr215=