Canonical Allele Identifier: CA383246941
Gene: KCNJ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128840070C>A , CM000673.2:g.128840070C>A GRCh38
NC_000011.9:g.128709965C>A , CM000673.1:g.128709965C>A GRCh37
NC_000011.8:g.128215175C>A NCBI36
NG_009379.1:g.32304G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000392666.6:c.174G>T MANE Select ENSP00000376434.1:p.Trp58Cys
ENST00000324003.3:c.174G>T ENSP00000316136.3:p.Trp58Cys
ENST00000324036.7:c.174G>T ENSP00000316233.3:p.Trp58Cys
ENST00000392664.2:c.231G>T ENSP00000376432.2:p.Trp77Cys
ENST00000392665.6:c.174G>T ENSP00000376433.2:p.Trp58Cys
ENST00000392666.5:c.174G>T ENSP00000376434.1:p.Trp58Cys
ENST00000440599.6:c.174G>T ENSP00000406320.2:p.Trp58Cys
ENST00000531562.1:n.519G>T
NM_000220.4:c.231G>T NP_000211.1:p.Trp77Cys
NM_153764.2:c.174G>T NP_722448.1:p.Trp58Cys
NM_153765.2:c.225G>T NP_722449.3:p.Trp75Cys
NM_153766.2:c.174G>T NP_722450.1:p.Trp58Cys
NM_153767.3:c.174G>T NP_722451.1:p.Trp58Cys
NM_000220.6:c.231G>T NP_000211.1:p.Trp77Cys
NM_153764.3:c.174G>T NP_722448.1:p.Trp58Cys
NM_153765.3:c.225G>T NP_722449.3:p.Trp75Cys
NM_153766.3:c.174G>T MANE Select NP_722450.1:p.Trp58Cys
NM_153767.4:c.174G>T NP_722451.1:p.Trp58Cys