Canonical Allele Identifier: CA2008293056
Gene: KCNJ5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128911997C= , CM000673.2:g.128911997C= GRCh38
NC_000011.9:g.128781892C= , CM000673.1:g.128781892C= GRCh37
NC_000011.8:g.128287102C= NCBI36
NG_023406.2:g.25580C= , LRG_333:g.25580C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529694.6:c.724C= MANE Select ENSP00000433295.1:p.Arg242=
ENST00000338350.4:c.724C= ENSP00000339960.4:p.Arg242=
ENST00000529694.5:c.724C= ENSP00000433295.1:p.Arg242=
ENST00000533599.1:c.724C= ENSP00000434266.1:p.Arg242=
NM_000890.3:c.724C= , LRG_333t1:c.724C= NP_000881.3:p.Arg242=
XM_011542809.1:c.724C= XP_011541111.1:p.Arg242=
XM_011542810.1:c.724C= XP_011541112.1:p.Arg242=
NM_000890.4:c.724C= NP_000881.3:p.Arg242=
NM_001354169.1:c.724C= NP_001341098.1:p.Arg242=
XM_011542809.2:c.724C= XP_011541111.1:p.Arg242=
XM_011542810.3:c.724C= XP_011541112.1:p.Arg242=
NM_000890.5:c.724C= MANE Select NP_000881.3:p.Arg242=
NM_001354169.2:c.724C= NP_001341098.1:p.Arg242=