Canonical Allele Identifier: CA1139821078
Community Standard Title: NM_014663.3(KDM4A):c.-40+1083G=
Gene: KDM4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43651335G= , CM000663.2:g.43651335G= GRCh38
NC_000001.10:g.44117006G= , CM000663.1:g.44117006G= GRCh37
NC_000001.9:g.43889593G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_014663.3:c.-40+1083G= MANE Select NP_055478.2:n.-40+1083G=
ENST00000372396.4:c.-40+1083G= MANE Select ENSP00000361473.3:n.-40+1083G=
NM_014663.2:c.-40+1083G= NP_055478.2:n.-40+1083G=
ENST00000372396.3:c.-40+1083G= ENSP00000361473.3:n.-40+1083G=
ENST00000463151.5:n.139+661G=
ENST00000645057.1:c.-40+1083G= ENSP00000494063.1:n.-40+1083G=
XM_005271354.2:c.-40+661G= XP_005271411.1:n.-40+661G=
XM_005271354.3:c.-40+661G= XP_005271411.1:n.-40+661G=
XM_005271355.2:c.-40+786G= XP_005271412.1:n.-40+786G=
XM_005271355.3:c.-40+786G= XP_005271412.1:n.-40+786G=
XM_005271356.2:c.-450+786G= XP_005271413.1:n.-450+786G=