Canonical Allele Identifier: CA2470919001
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707948C= , CM000686.2:g.19707948C= GRCh38
NC_000024.9:g.21869834C= , CM000686.1:g.21869834C= GRCh37
NC_000024.8:g.20329222C= NCBI36
NG_032920.1:g.41992G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3385G= MANE Select ENSP00000322408.4:p.Asp1129=
ENST00000317961.8:c.3385G= ENSP00000322408.4:p.Asp1129=
ENST00000382806.6:c.3214G= ENSP00000372256.2:p.Asp1072=
ENST00000415360.1:c.301G= ENSP00000389433.1:p.Asp101=
ENST00000440077.5:c.3262G= ENSP00000398543.1:p.Asp1088=
ENST00000469599.6:n.1983G=
ENST00000492117.1:n.3277G=
ENST00000541639.5:c.3478G= ENSP00000444293.1:p.Asp1160=
NM_001146705.1:c.3478G= NP_001140177.1:p.Asp1160=
NM_001146706.1:c.3214G= NP_001140178.1:p.Asp1072=
NM_004653.4:c.3385G= NP_004644.2:p.Asp1129=
XM_005262560.1:c.3250G= XP_005262617.1:p.Asp1084=
XM_005262561.1:c.3154G= XP_005262618.1:p.Asp1052=
XM_011531468.1:c.3307G= XP_011529770.1:p.Asp1103=
XR_244571.2:n.3673G=
XR_430568.2:n.4007G=
XM_005262560.3:c.3250G= XP_005262617.1:p.Asp1084=
XM_005262561.3:c.3154G= XP_005262618.1:p.Asp1052=
XM_011531468.3:c.3307G= XP_011529770.1:p.Asp1103=
XM_024452495.1:c.1375G= XP_024308263.1:p.Asp459=
XM_024452496.1:c.1141G= XP_024308264.1:p.Asp381=
XR_001756009.2:n.4123G=
XR_001756010.2:n.4123G=
XR_001756011.2:n.3988G=
XR_001756012.2:n.4136G=
XR_001756013.2:n.3454G=
XR_002958832.1:n.3555G=
XR_002958834.1:n.3779G=
XR_002958835.1:n.3662G=
XR_002958836.1:n.4345G=
XR_002958837.1:n.4152G=
XR_244571.4:n.3672G=
XR_430568.4:n.4006G=
NM_001146706.2:c.3214G= NP_001140178.1:p.Asp1072=
NM_004653.5:c.3385G= MANE Select NP_004644.2:p.Asp1129=
NM_001146705.2:c.3478G= NP_001140177.1:p.Asp1160=