Canonical Allele Identifier: CA2470918950
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707439C= , CM000686.2:g.19707439C= GRCh38
NC_000024.9:g.21869325C= , CM000686.1:g.21869325C= GRCh37
NC_000024.8:g.20328713C= NCBI36
NG_032920.1:g.42501G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3707G= MANE Select ENSP00000322408.4:p.Arg1236=
ENST00000317961.8:c.3707G= ENSP00000322408.4:p.Arg1236=
ENST00000382806.6:c.3536G= ENSP00000372256.2:p.Arg1179=
ENST00000415360.1:c.623G= ENSP00000389433.1:p.Arg208=
ENST00000440077.5:c.3584G= ENSP00000398543.1:p.Arg1195=
ENST00000469599.6:n.2305G=
ENST00000492117.1:n.3599G=
ENST00000541639.5:c.3800G= ENSP00000444293.1:p.Arg1267=
NM_001146705.1:c.3800G= NP_001140177.1:p.Arg1267=
NM_001146706.1:c.3536G= NP_001140178.1:p.Arg1179=
NM_004653.4:c.3707G= NP_004644.2:p.Arg1236=
XM_005262560.1:c.3572G= XP_005262617.1:p.Arg1191=
XM_005262561.1:c.3476G= XP_005262618.1:p.Arg1159=
XM_011531468.1:c.3629G= XP_011529770.1:p.Arg1210=
XR_244571.2:n.3995G=
XR_430568.2:n.4329G=
XM_005262560.3:c.3572G= XP_005262617.1:p.Arg1191=
XM_005262561.3:c.3476G= XP_005262618.1:p.Arg1159=
XM_011531468.3:c.3629G= XP_011529770.1:p.Arg1210=
XM_024452495.1:c.1697G= XP_024308263.1:p.Arg566=
XM_024452496.1:c.1463G= XP_024308264.1:p.Arg488=
XR_001756009.2:n.4445G=
XR_001756010.2:n.4445G=
XR_001756011.2:n.4310G=
XR_001756012.2:n.4458G=
XR_001756013.2:n.3776G=
XR_002958832.1:n.3877G=
XR_002958834.1:n.4101G=
XR_002958835.1:n.3984G=
XR_002958836.1:n.4667G=
XR_002958837.1:n.4474G=
XR_244571.4:n.3994G=
XR_430568.4:n.4328G=
NM_001146706.2:c.3536G= NP_001140178.1:p.Arg1179=
NM_004653.5:c.3707G= MANE Select NP_004644.2:p.Arg1236=
NM_001146705.2:c.3800G= NP_001140177.1:p.Arg1267=