Canonical Allele Identifier: CA477703370
Gene: KCNJ1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.128709647G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128839752G>C , CM000673.2:g.128839752G>C GRCh38
NC_000011.9:g.128709647G>C , CM000673.1:g.128709647G>C GRCh37
NC_000011.8:g.128214857G>C NCBI36
NG_009379.1:g.32622C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000392666.6:c.492C>G MANE Select ENSP00000376434.1:p.Ser164=
ENST00000324036.7:c.492C>G ENSP00000316233.3:p.Ser164=
ENST00000392664.2:c.549C>G ENSP00000376432.2:p.Ser183=
ENST00000392665.6:c.492C>G ENSP00000376433.2:p.Ser164=
ENST00000392666.5:c.492C>G ENSP00000376434.1:p.Ser164=
ENST00000440599.6:c.492C>G ENSP00000406320.2:p.Ser164=
NM_000220.4:c.549C>G NP_000211.1:p.Ser183=
NM_153764.2:c.492C>G NP_722448.1:p.Ser164=
NM_153765.2:c.543C>G NP_722449.3:p.Ser181=
NM_153766.2:c.492C>G NP_722450.1:p.Ser164=
NM_153767.3:c.492C>G NP_722451.1:p.Ser164=
NM_000220.6:c.549C>G NP_000211.1:p.Ser183=
NM_153764.3:c.492C>G NP_722448.1:p.Ser164=
NM_153765.3:c.543C>G NP_722449.3:p.Ser181=
NM_153766.3:c.492C>G MANE Select NP_722450.1:p.Ser164=
NM_153767.4:c.492C>G NP_722451.1:p.Ser164=