Canonical Allele Identifier: CA2470919011
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19708035T= , CM000686.2:g.19708035T= GRCh38
NC_000024.9:g.21869921T= , CM000686.1:g.21869921T= GRCh37
NC_000024.8:g.20329309T= NCBI36
NG_032920.1:g.41905A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3298A= MANE Select ENSP00000322408.4:p.Thr1100=
ENST00000317961.8:c.3298A= ENSP00000322408.4:p.Thr1100=
ENST00000382806.6:c.3127A= ENSP00000372256.2:p.Thr1043=
ENST00000415360.1:c.214A= ENSP00000389433.1:p.Thr72=
ENST00000440077.5:c.3175A= ENSP00000398543.1:p.Thr1059=
ENST00000469599.6:n.1896A=
ENST00000492117.1:n.3190A=
ENST00000541639.5:c.3391A= ENSP00000444293.1:p.Thr1131=
NM_001146705.1:c.3391A= NP_001140177.1:p.Thr1131=
NM_001146706.1:c.3127A= NP_001140178.1:p.Thr1043=
NM_004653.4:c.3298A= NP_004644.2:p.Thr1100=
XM_005262560.1:c.3163A= XP_005262617.1:p.Thr1055=
XM_005262561.1:c.3067A= XP_005262618.1:p.Thr1023=
XM_011531468.1:c.3220A= XP_011529770.1:p.Thr1074=
XR_244571.2:n.3586A=
XR_430568.2:n.3920A=
XM_005262560.3:c.3163A= XP_005262617.1:p.Thr1055=
XM_005262561.3:c.3067A= XP_005262618.1:p.Thr1023=
XM_011531468.3:c.3220A= XP_011529770.1:p.Thr1074=
XM_024452495.1:c.1288A= XP_024308263.1:p.Thr430=
XM_024452496.1:c.1054A= XP_024308264.1:p.Thr352=
XR_001756009.2:n.4036A=
XR_001756010.2:n.4036A=
XR_001756011.2:n.3901A=
XR_001756012.2:n.4049A=
XR_001756013.2:n.3367A=
XR_002958832.1:n.3468A=
XR_002958834.1:n.3692A=
XR_002958835.1:n.3575A=
XR_002958836.1:n.4258A=
XR_002958837.1:n.4065A=
XR_244571.4:n.3585A=
XR_430568.4:n.3919A=
NM_001146706.2:c.3127A= NP_001140178.1:p.Thr1043=
NM_004653.5:c.3298A= MANE Select NP_004644.2:p.Thr1100=
NM_001146705.2:c.3391A= NP_001140177.1:p.Thr1131=