Canonical Allele Identifier: CA2470918955
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707497A= , CM000686.2:g.19707497A= GRCh38
NC_000024.9:g.21869383A= , CM000686.1:g.21869383A= GRCh37
NC_000024.8:g.20328771A= NCBI36
NG_032920.1:g.42443T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3649T= MANE Select ENSP00000322408.4:p.Ser1217=
ENST00000317961.8:c.3649T= ENSP00000322408.4:p.Ser1217=
ENST00000382806.6:c.3478T= ENSP00000372256.2:p.Ser1160=
ENST00000415360.1:c.565T= ENSP00000389433.1:p.Ser189=
ENST00000440077.5:c.3526T= ENSP00000398543.1:p.Ser1176=
ENST00000469599.6:n.2247T=
ENST00000492117.1:n.3541T=
ENST00000541639.5:c.3742T= ENSP00000444293.1:p.Ser1248=
NM_001146705.1:c.3742T= NP_001140177.1:p.Ser1248=
NM_001146706.1:c.3478T= NP_001140178.1:p.Ser1160=
NM_004653.4:c.3649T= NP_004644.2:p.Ser1217=
XM_005262560.1:c.3514T= XP_005262617.1:p.Ser1172=
XM_005262561.1:c.3418T= XP_005262618.1:p.Ser1140=
XM_011531468.1:c.3571T= XP_011529770.1:p.Ser1191=
XR_244571.2:n.3937T=
XR_430568.2:n.4271T=
XM_005262560.3:c.3514T= XP_005262617.1:p.Ser1172=
XM_005262561.3:c.3418T= XP_005262618.1:p.Ser1140=
XM_011531468.3:c.3571T= XP_011529770.1:p.Ser1191=
XM_024452495.1:c.1639T= XP_024308263.1:p.Ser547=
XM_024452496.1:c.1405T= XP_024308264.1:p.Ser469=
XR_001756009.2:n.4387T=
XR_001756010.2:n.4387T=
XR_001756011.2:n.4252T=
XR_001756012.2:n.4400T=
XR_001756013.2:n.3718T=
XR_002958832.1:n.3819T=
XR_002958834.1:n.4043T=
XR_002958835.1:n.3926T=
XR_002958836.1:n.4609T=
XR_002958837.1:n.4416T=
XR_244571.4:n.3936T=
XR_430568.4:n.4270T=
NM_001146706.2:c.3478T= NP_001140178.1:p.Ser1160=
NM_004653.5:c.3649T= MANE Select NP_004644.2:p.Ser1217=
NM_001146705.2:c.3742T= NP_001140177.1:p.Ser1248=