Canonical Allele Identifier: CA2008294704
Gene: KCNJ5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128916284A= , CM000673.2:g.128916284A= GRCh38
NC_000011.9:g.128786179A= , CM000673.1:g.128786179A= GRCh37
NC_000011.8:g.128291389A= NCBI36
NG_023406.2:g.29867A= , LRG_333:g.29867A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529694.6:c.938-125A= MANE Select ENSP00000433295.1:n.938-125A=
ENST00000338350.4:c.938-125A= ENSP00000339960.4:n.938-125A=
ENST00000529694.5:c.938-125A= ENSP00000433295.1:n.938-125A=
ENST00000533599.1:c.938-125A= ENSP00000434266.1:n.938-125A=
NM_000890.3:c.938-125A= , LRG_333t1:c.938-125A= NP_000881.3:n.938-125A=
XM_011542809.1:c.938-125A= XP_011541111.1:n.938-125A=
XM_011542810.1:c.938-125A= XP_011541112.1:n.938-125A=
NM_000890.4:c.938-125A= NP_000881.3:n.938-125A=
NM_001354169.1:c.938-125A= NP_001341098.1:n.938-125A=
XM_011542809.2:c.938-125A= XP_011541111.1:n.938-125A=
XM_011542810.3:c.938-125A= XP_011541112.1:n.938-125A=
NM_000890.5:c.938-125A= MANE Select NP_000881.3:n.938-125A=
NM_001354169.2:c.938-125A= NP_001341098.1:n.938-125A=