Canonical Allele Identifier: CA383244652
Gene: KCNJ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128839631T>G , CM000673.2:g.128839631T>G GRCh38
NC_000011.9:g.128709526T>G , CM000673.1:g.128709526T>G GRCh37
NC_000011.8:g.128214736T>G NCBI36
NG_009379.1:g.32743A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000392666.6:c.613A>C MANE Select ENSP00000376434.1:p.Ser205Arg
ENST00000324036.7:c.613A>C ENSP00000316233.3:p.Ser205Arg
ENST00000392664.2:c.670A>C ENSP00000376432.2:p.Ser224Arg
ENST00000392665.6:c.613A>C ENSP00000376433.2:p.Ser205Arg
ENST00000392666.5:c.613A>C ENSP00000376434.1:p.Ser205Arg
ENST00000440599.6:c.613A>C ENSP00000406320.2:p.Ser205Arg
NM_000220.4:c.670A>C NP_000211.1:p.Ser224Arg
NM_153764.2:c.613A>C NP_722448.1:p.Ser205Arg
NM_153765.2:c.664A>C NP_722449.3:p.Ser222Arg
NM_153766.2:c.613A>C NP_722450.1:p.Ser205Arg
NM_153767.3:c.613A>C NP_722451.1:p.Ser205Arg
NM_000220.6:c.670A>C NP_000211.1:p.Ser224Arg
NM_153764.3:c.613A>C NP_722448.1:p.Ser205Arg
NM_153765.3:c.664A>C NP_722449.3:p.Ser222Arg
NM_153766.3:c.613A>C MANE Select NP_722450.1:p.Ser205Arg
NM_153767.4:c.613A>C NP_722451.1:p.Ser205Arg