Canonical Allele Identifier: CA2470918951
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707444A= , CM000686.2:g.19707444A= GRCh38
NC_000024.9:g.21869330A= , CM000686.1:g.21869330A= GRCh37
NC_000024.8:g.20328718A= NCBI36
NG_032920.1:g.42496T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3702T= MANE Select ENSP00000322408.4:p.Cys1234=
ENST00000317961.8:c.3702T= ENSP00000322408.4:p.Cys1234=
ENST00000382806.6:c.3531T= ENSP00000372256.2:p.Cys1177=
ENST00000415360.1:c.618T= ENSP00000389433.1:p.Cys206=
ENST00000440077.5:c.3579T= ENSP00000398543.1:p.Cys1193=
ENST00000469599.6:n.2300T=
ENST00000492117.1:n.3594T=
ENST00000541639.5:c.3795T= ENSP00000444293.1:p.Cys1265=
NM_001146705.1:c.3795T= NP_001140177.1:p.Cys1265=
NM_001146706.1:c.3531T= NP_001140178.1:p.Cys1177=
NM_004653.4:c.3702T= NP_004644.2:p.Cys1234=
XM_005262560.1:c.3567T= XP_005262617.1:p.Cys1189=
XM_005262561.1:c.3471T= XP_005262618.1:p.Cys1157=
XM_011531468.1:c.3624T= XP_011529770.1:p.Cys1208=
XR_244571.2:n.3990T=
XR_430568.2:n.4324T=
XM_005262560.3:c.3567T= XP_005262617.1:p.Cys1189=
XM_005262561.3:c.3471T= XP_005262618.1:p.Cys1157=
XM_011531468.3:c.3624T= XP_011529770.1:p.Cys1208=
XM_024452495.1:c.1692T= XP_024308263.1:p.Cys564=
XM_024452496.1:c.1458T= XP_024308264.1:p.Cys486=
XR_001756009.2:n.4440T=
XR_001756010.2:n.4440T=
XR_001756011.2:n.4305T=
XR_001756012.2:n.4453T=
XR_001756013.2:n.3771T=
XR_002958832.1:n.3872T=
XR_002958834.1:n.4096T=
XR_002958835.1:n.3979T=
XR_002958836.1:n.4662T=
XR_002958837.1:n.4469T=
XR_244571.4:n.3989T=
XR_430568.4:n.4323T=
NM_001146706.2:c.3531T= NP_001140178.1:p.Cys1177=
NM_004653.5:c.3702T= MANE Select NP_004644.2:p.Cys1234=
NM_001146705.2:c.3795T= NP_001140177.1:p.Cys1265=