Canonical Allele Identifier: CA2470918948
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707430C= , CM000686.2:g.19707430C= GRCh38
NC_000024.9:g.21869316C= , CM000686.1:g.21869316C= GRCh37
NC_000024.8:g.20328704C= NCBI36
NG_032920.1:g.42510G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3716G= MANE Select ENSP00000322408.4:p.Arg1239=
ENST00000317961.8:c.3716G= ENSP00000322408.4:p.Arg1239=
ENST00000382806.6:c.3545G= ENSP00000372256.2:p.Arg1182=
ENST00000415360.1:c.632G= ENSP00000389433.1:p.Arg211=
ENST00000440077.5:c.3593G= ENSP00000398543.1:p.Arg1198=
ENST00000469599.6:n.2314G=
ENST00000492117.1:n.3608G=
ENST00000541639.5:c.3809G= ENSP00000444293.1:p.Arg1270=
NM_001146705.1:c.3809G= NP_001140177.1:p.Arg1270=
NM_001146706.1:c.3545G= NP_001140178.1:p.Arg1182=
NM_004653.4:c.3716G= NP_004644.2:p.Arg1239=
XM_005262560.1:c.3581G= XP_005262617.1:p.Arg1194=
XM_005262561.1:c.3485G= XP_005262618.1:p.Arg1162=
XM_011531468.1:c.3638G= XP_011529770.1:p.Arg1213=
XR_244571.2:n.4004G=
XR_430568.2:n.4338G=
XM_005262560.3:c.3581G= XP_005262617.1:p.Arg1194=
XM_005262561.3:c.3485G= XP_005262618.1:p.Arg1162=
XM_011531468.3:c.3638G= XP_011529770.1:p.Arg1213=
XM_024452495.1:c.1706G= XP_024308263.1:p.Arg569=
XM_024452496.1:c.1472G= XP_024308264.1:p.Arg491=
XR_001756009.2:n.4454G=
XR_001756010.2:n.4454G=
XR_001756011.2:n.4319G=
XR_001756012.2:n.4467G=
XR_001756013.2:n.3785G=
XR_002958832.1:n.3886G=
XR_002958834.1:n.4110G=
XR_002958835.1:n.3993G=
XR_002958836.1:n.4676G=
XR_002958837.1:n.4483G=
XR_244571.4:n.4003G=
XR_430568.4:n.4337G=
NM_001146706.2:c.3545G= NP_001140178.1:p.Arg1182=
NM_004653.5:c.3716G= MANE Select NP_004644.2:p.Arg1239=
NM_001146705.2:c.3809G= NP_001140177.1:p.Arg1270=