Canonical Allele Identifier: CA2470918876

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706841C= , CM000686.2:g.19706841C=	GRCh38
NC_000024.9:g.21868727C= , CM000686.1:g.21868727C=	GRCh37
NC_000024.8:g.20328115C=	NCBI36
NG_032920.1:g.43099G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4022G= MANE Select	ENSP00000322408.4:p.Gly1341=
ENST00000317961.8:c.4022G=	ENSP00000322408.4:p.Gly1341=
ENST00000382806.6:c.3851G=	ENSP00000372256.2:p.Gly1284=
ENST00000440077.5:c.3899G=	ENSP00000398543.1:p.Gly1300=
ENST00000469599.6:n.2620G=
ENST00000492117.1:n.3914G=
ENST00000541639.5:c.4115G=	ENSP00000444293.1:p.Gly1372=
NM_001146705.1:c.4115G=	NP_001140177.1:p.Gly1372=
NM_001146706.1:c.3851G=	NP_001140178.1:p.Gly1284=
NM_004653.4:c.4022G=	NP_004644.2:p.Gly1341=
XM_005262560.1:c.3887G=	XP_005262617.1:p.Gly1296=
XM_005262561.1:c.3791G=	XP_005262618.1:p.Gly1264=
XM_011531468.1:c.3944G=	XP_011529770.1:p.Gly1315=
XR_244571.2:n.4310G=
XR_430568.2:n.4644G=
XM_005262560.3:c.3887G=	XP_005262617.1:p.Gly1296=
XM_005262561.3:c.3791G=	XP_005262618.1:p.Gly1264=
XM_011531468.3:c.3944G=	XP_011529770.1:p.Gly1315=
XM_024452495.1:c.2012G=	XP_024308263.1:p.Gly671=
XM_024452496.1:c.1778G=	XP_024308264.1:p.Gly593=
XR_001756009.2:n.4760G=
XR_001756010.2:n.4760G=
XR_001756011.2:n.4625G=
XR_001756012.2:n.4773G=
XR_001756013.2:n.4091G=
XR_002958832.1:n.4192G=
XR_002958834.1:n.4416G=
XR_002958835.1:n.4299G=
XR_002958836.1:n.4982G=
XR_002958837.1:n.4789G=
XR_244571.4:n.4309G=
XR_430568.4:n.4643G=
NM_001146706.2:c.3851G=	NP_001140178.1:p.Gly1284=
NM_004653.5:c.4022G= MANE Select	NP_004644.2:p.Gly1341=
NM_001146705.2:c.4115G=	NP_001140177.1:p.Gly1372=