Canonical Allele Identifier: CA2470918769
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19706085G= , CM000686.2:g.19706085G= GRCh38
NC_000024.9:g.21867971G= , CM000686.1:g.21867971G= GRCh37
NC_000024.8:g.20327359G= NCBI36
NG_032920.1:g.43855C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.4530C= MANE Select ENSP00000322408.4:p.Ser1510=
ENST00000317961.8:c.4530C= ENSP00000322408.4:p.Ser1510=
ENST00000382806.6:c.4359C= ENSP00000372256.2:p.Ser1453=
ENST00000440077.5:c.4407C= ENSP00000398543.1:p.Ser1469=
ENST00000469599.6:n.3281C=
ENST00000492117.1:n.4575C=
ENST00000541639.5:c.4623C= ENSP00000444293.1:p.Ser1541=
NM_001146705.1:c.4623C= NP_001140177.1:p.Ser1541=
NM_001146706.1:c.4359C= NP_001140178.1:p.Ser1453=
NM_004653.4:c.4530C= NP_004644.2:p.Ser1510=
XM_005262560.1:c.4395C= XP_005262617.1:p.Ser1465=
XM_005262561.1:c.4299C= XP_005262618.1:p.Ser1433=
XM_011531468.1:c.4452C= XP_011529770.1:p.Ser1484=
XR_430568.2:n.5305C=
XM_005262560.3:c.4395C= XP_005262617.1:p.Ser1465=
XM_005262561.3:c.4299C= XP_005262618.1:p.Ser1433=
XM_011531468.3:c.4452C= XP_011529770.1:p.Ser1484=
XM_024452495.1:c.2520C= XP_024308263.1:p.Ser840=
XM_024452496.1:c.2286C= XP_024308264.1:p.Ser762=
XR_001756009.2:n.5268C=
XR_001756010.2:n.5236C=
XR_001756011.2:n.5133C=
XR_001756012.2:n.5281C=
XR_001756013.2:n.4599C=
XR_002958832.1:n.4853C=
XR_002958834.1:n.4924C=
XR_002958835.1:n.4807C=
XR_002958836.1:n.5458C=
XR_002958837.1:n.5265C=
XR_244571.4:n.4785C=
XR_430568.4:n.5304C=
NM_001146706.2:c.4359C= NP_001140178.1:p.Ser1453=
NM_004653.5:c.4530C= MANE Select NP_004644.2:p.Ser1510=
NM_001146705.2:c.4623C= NP_001140177.1:p.Ser1541=