Canonical Allele Identifier: CA2470918949
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707433C= , CM000686.2:g.19707433C= GRCh38
NC_000024.9:g.21869319C= , CM000686.1:g.21869319C= GRCh37
NC_000024.8:g.20328707C= NCBI36
NG_032920.1:g.42507G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3713G= MANE Select ENSP00000322408.4:p.Arg1238=
ENST00000317961.8:c.3713G= ENSP00000322408.4:p.Arg1238=
ENST00000382806.6:c.3542G= ENSP00000372256.2:p.Arg1181=
ENST00000415360.1:c.629G= ENSP00000389433.1:p.Arg210=
ENST00000440077.5:c.3590G= ENSP00000398543.1:p.Arg1197=
ENST00000469599.6:n.2311G=
ENST00000492117.1:n.3605G=
ENST00000541639.5:c.3806G= ENSP00000444293.1:p.Arg1269=
NM_001146705.1:c.3806G= NP_001140177.1:p.Arg1269=
NM_001146706.1:c.3542G= NP_001140178.1:p.Arg1181=
NM_004653.4:c.3713G= NP_004644.2:p.Arg1238=
XM_005262560.1:c.3578G= XP_005262617.1:p.Arg1193=
XM_005262561.1:c.3482G= XP_005262618.1:p.Arg1161=
XM_011531468.1:c.3635G= XP_011529770.1:p.Arg1212=
XR_244571.2:n.4001G=
XR_430568.2:n.4335G=
XM_005262560.3:c.3578G= XP_005262617.1:p.Arg1193=
XM_005262561.3:c.3482G= XP_005262618.1:p.Arg1161=
XM_011531468.3:c.3635G= XP_011529770.1:p.Arg1212=
XM_024452495.1:c.1703G= XP_024308263.1:p.Arg568=
XM_024452496.1:c.1469G= XP_024308264.1:p.Arg490=
XR_001756009.2:n.4451G=
XR_001756010.2:n.4451G=
XR_001756011.2:n.4316G=
XR_001756012.2:n.4464G=
XR_001756013.2:n.3782G=
XR_002958832.1:n.3883G=
XR_002958834.1:n.4107G=
XR_002958835.1:n.3990G=
XR_002958836.1:n.4673G=
XR_002958837.1:n.4480G=
XR_244571.4:n.4000G=
XR_430568.4:n.4334G=
NM_001146706.2:c.3542G= NP_001140178.1:p.Arg1181=
NM_004653.5:c.3713G= MANE Select NP_004644.2:p.Arg1238=
NM_001146705.2:c.3806G= NP_001140177.1:p.Arg1269=