Canonical Allele Identifier: CA2470918954
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707470C= , CM000686.2:g.19707470C= GRCh38
NC_000024.9:g.21869356C= , CM000686.1:g.21869356C= GRCh37
NC_000024.8:g.20328744C= NCBI36
NG_032920.1:g.42470G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3676G= MANE Select ENSP00000322408.4:p.Asp1226=
ENST00000317961.8:c.3676G= ENSP00000322408.4:p.Asp1226=
ENST00000382806.6:c.3505G= ENSP00000372256.2:p.Asp1169=
ENST00000415360.1:c.592G= ENSP00000389433.1:p.Asp198=
ENST00000440077.5:c.3553G= ENSP00000398543.1:p.Asp1185=
ENST00000469599.6:n.2274G=
ENST00000492117.1:n.3568G=
ENST00000541639.5:c.3769G= ENSP00000444293.1:p.Asp1257=
NM_001146705.1:c.3769G= NP_001140177.1:p.Asp1257=
NM_001146706.1:c.3505G= NP_001140178.1:p.Asp1169=
NM_004653.4:c.3676G= NP_004644.2:p.Asp1226=
XM_005262560.1:c.3541G= XP_005262617.1:p.Asp1181=
XM_005262561.1:c.3445G= XP_005262618.1:p.Asp1149=
XM_011531468.1:c.3598G= XP_011529770.1:p.Asp1200=
XR_244571.2:n.3964G=
XR_430568.2:n.4298G=
XM_005262560.3:c.3541G= XP_005262617.1:p.Asp1181=
XM_005262561.3:c.3445G= XP_005262618.1:p.Asp1149=
XM_011531468.3:c.3598G= XP_011529770.1:p.Asp1200=
XM_024452495.1:c.1666G= XP_024308263.1:p.Asp556=
XM_024452496.1:c.1432G= XP_024308264.1:p.Asp478=
XR_001756009.2:n.4414G=
XR_001756010.2:n.4414G=
XR_001756011.2:n.4279G=
XR_001756012.2:n.4427G=
XR_001756013.2:n.3745G=
XR_002958832.1:n.3846G=
XR_002958834.1:n.4070G=
XR_002958835.1:n.3953G=
XR_002958836.1:n.4636G=
XR_002958837.1:n.4443G=
XR_244571.4:n.3963G=
XR_430568.4:n.4297G=
NM_001146706.2:c.3505G= NP_001140178.1:p.Asp1169=
NM_004653.5:c.3676G= MANE Select NP_004644.2:p.Asp1226=
NM_001146705.2:c.3769G= NP_001140177.1:p.Asp1257=