Canonical Allele Identifier: CA477703267

Gene: KCNJ1

Linked Data

• ClinVar Variation Id: 2697231
• ClinVar RCV Id: RCV003549176
• MyVariant Identifiers: chr11:g.128709938T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128840043T>G , CM000673.2:g.128840043T>G	GRCh38
NC_000011.9:g.128709938T>G , CM000673.1:g.128709938T>G	GRCh37
NC_000011.8:g.128215148T>G	NCBI36
NG_009379.1:g.32331A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.201A>C MANE Select	ENSP00000376434.1:p.Thr67=
ENST00000324003.3:c.201A>C	ENSP00000316136.3:p.Thr67=
ENST00000324036.7:c.201A>C	ENSP00000316233.3:p.Thr67=
ENST00000392664.2:c.258A>C	ENSP00000376432.2:p.Thr86=
ENST00000392665.6:c.201A>C	ENSP00000376433.2:p.Thr67=
ENST00000392666.5:c.201A>C	ENSP00000376434.1:p.Thr67=
ENST00000440599.6:c.201A>C	ENSP00000406320.2:p.Thr67=
NM_000220.4:c.258A>C	NP_000211.1:p.Thr86=
NM_153764.2:c.201A>C	NP_722448.1:p.Thr67=
NM_153765.2:c.252A>C	NP_722449.3:p.Thr84=
NM_153766.2:c.201A>C	NP_722450.1:p.Thr67=
NM_153767.3:c.201A>C	NP_722451.1:p.Thr67=
NM_000220.6:c.258A>C	NP_000211.1:p.Thr86=
NM_153764.3:c.201A>C	NP_722448.1:p.Thr67=
NM_153765.3:c.252A>C	NP_722449.3:p.Thr84=
NM_153766.3:c.201A>C MANE Select	NP_722450.1:p.Thr67=
NM_153767.4:c.201A>C	NP_722451.1:p.Thr67=