Canonical Allele Identifier: CA2008294938
Gene: KCNJ5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128916758G= , CM000673.2:g.128916758G= GRCh38
NC_000011.9:g.128786653G= , CM000673.1:g.128786653G= GRCh37
NC_000011.8:g.128291863G= NCBI36
NG_023406.2:g.30341G= , LRG_333:g.30341G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529694.6:c.*27G= MANE Select ENSP00000433295.1:n.*27G=
ENST00000338350.4:c.*27G= ENSP00000339960.4:n.*27G=
ENST00000529694.5:c.*27G= ENSP00000433295.1:n.*27G=
NM_000890.3:c.*27G= , LRG_333t1:c.*27G= NP_000881.3:n.*27G=
XM_011542809.1:c.*27G= XP_011541111.1:n.*27G=
XM_011542810.1:c.*27G= XP_011541112.1:n.*27G=
NM_000890.4:c.*27G= NP_000881.3:n.*27G=
NM_001354169.1:c.*27G= NP_001341098.1:n.*27G=
XM_011542809.2:c.*27G= XP_011541111.1:n.*27G=
XM_011542810.3:c.*27G= XP_011541112.1:n.*27G=
NM_000890.5:c.*27G= MANE Select NP_000881.3:n.*27G=
NM_001354169.2:c.*27G= NP_001341098.1:n.*27G=