Canonical Allele Identifier: CA477703009

Gene: KCNJ1

Linked Data

• MyVariant Identifiers: chr11:g.128709293C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128839398C>G , CM000673.2:g.128839398C>G	GRCh38
NC_000011.9:g.128709293C>G , CM000673.1:g.128709293C>G	GRCh37
NC_000011.8:g.128214503C>G	NCBI36
NG_009379.1:g.32976G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.846G>C MANE Select	ENSP00000376434.1:p.Val282=
ENST00000324036.7:c.846G>C	ENSP00000316233.3:p.Val282=
ENST00000392664.2:c.903G>C	ENSP00000376432.2:p.Val301=
ENST00000392665.6:c.846G>C	ENSP00000376433.2:p.Val282=
ENST00000392666.5:c.846G>C	ENSP00000376434.1:p.Val282=
ENST00000440599.6:c.846G>C	ENSP00000406320.2:p.Val282=
NM_000220.4:c.903G>C	NP_000211.1:p.Val301=
NM_153764.2:c.846G>C	NP_722448.1:p.Val282=
NM_153765.2:c.897G>C	NP_722449.3:p.Val299=
NM_153766.2:c.846G>C	NP_722450.1:p.Val282=
NM_153767.3:c.846G>C	NP_722451.1:p.Val282=
NM_000220.6:c.903G>C	NP_000211.1:p.Val301=
NM_153764.3:c.846G>C	NP_722448.1:p.Val282=
NM_153765.3:c.897G>C	NP_722449.3:p.Val299=
NM_153766.3:c.846G>C MANE Select	NP_722450.1:p.Val282=
NM_153767.4:c.846G>C	NP_722451.1:p.Val282=