Canonical Allele Identifier: CA2470918947
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707429C= , CM000686.2:g.19707429C= GRCh38
NC_000024.9:g.21869315C= , CM000686.1:g.21869315C= GRCh37
NC_000024.8:g.20328703C= NCBI36
NG_032920.1:g.42511G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3717G= MANE Select ENSP00000322408.4:p.Arg1239=
ENST00000317961.8:c.3717G= ENSP00000322408.4:p.Arg1239=
ENST00000382806.6:c.3546G= ENSP00000372256.2:p.Arg1182=
ENST00000415360.1:c.633G= ENSP00000389433.1:p.Arg211=
ENST00000440077.5:c.3594G= ENSP00000398543.1:p.Arg1198=
ENST00000469599.6:n.2315G=
ENST00000492117.1:n.3609G=
ENST00000541639.5:c.3810G= ENSP00000444293.1:p.Arg1270=
NM_001146705.1:c.3810G= NP_001140177.1:p.Arg1270=
NM_001146706.1:c.3546G= NP_001140178.1:p.Arg1182=
NM_004653.4:c.3717G= NP_004644.2:p.Arg1239=
XM_005262560.1:c.3582G= XP_005262617.1:p.Arg1194=
XM_005262561.1:c.3486G= XP_005262618.1:p.Arg1162=
XM_011531468.1:c.3639G= XP_011529770.1:p.Arg1213=
XR_244571.2:n.4005G=
XR_430568.2:n.4339G=
XM_005262560.3:c.3582G= XP_005262617.1:p.Arg1194=
XM_005262561.3:c.3486G= XP_005262618.1:p.Arg1162=
XM_011531468.3:c.3639G= XP_011529770.1:p.Arg1213=
XM_024452495.1:c.1707G= XP_024308263.1:p.Arg569=
XM_024452496.1:c.1473G= XP_024308264.1:p.Arg491=
XR_001756009.2:n.4455G=
XR_001756010.2:n.4455G=
XR_001756011.2:n.4320G=
XR_001756012.2:n.4468G=
XR_001756013.2:n.3786G=
XR_002958832.1:n.3887G=
XR_002958834.1:n.4111G=
XR_002958835.1:n.3994G=
XR_002958836.1:n.4677G=
XR_002958837.1:n.4484G=
XR_244571.4:n.4004G=
XR_430568.4:n.4338G=
NM_001146706.2:c.3546G= NP_001140178.1:p.Arg1182=
NM_004653.5:c.3717G= MANE Select NP_004644.2:p.Arg1239=
NM_001146705.2:c.3810G= NP_001140177.1:p.Arg1270=