Canonical Allele Identifier: CA2470918768

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706076G= , CM000686.2:g.19706076G=	GRCh38
NC_000024.9:g.21867962G= , CM000686.1:g.21867962G=	GRCh37
NC_000024.8:g.20327350G=	NCBI36
NG_032920.1:g.43864C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4539C= MANE Select	ENSP00000322408.4:p.His1513=
ENST00000317961.8:c.4539C=	ENSP00000322408.4:p.His1513=
ENST00000382806.6:c.4368C=	ENSP00000372256.2:p.His1456=
ENST00000440077.5:c.4416C=	ENSP00000398543.1:p.His1472=
ENST00000469599.6:n.3290C=
ENST00000492117.1:n.4584C=
ENST00000541639.5:c.4632C=	ENSP00000444293.1:p.His1544=
NM_001146705.1:c.4632C=	NP_001140177.1:p.His1544=
NM_001146706.1:c.4368C=	NP_001140178.1:p.His1456=
NM_004653.4:c.4539C=	NP_004644.2:p.His1513=
XM_005262560.1:c.4404C=	XP_005262617.1:p.His1468=
XM_005262561.1:c.4308C=	XP_005262618.1:p.His1436=
XM_011531468.1:c.4461C=	XP_011529770.1:p.His1487=
XR_430568.2:n.5314C=
XM_005262560.3:c.4404C=	XP_005262617.1:p.His1468=
XM_005262561.3:c.4308C=	XP_005262618.1:p.His1436=
XM_011531468.3:c.4461C=	XP_011529770.1:p.His1487=
XM_024452495.1:c.2529C=	XP_024308263.1:p.His843=
XM_024452496.1:c.2295C=	XP_024308264.1:p.His765=
XR_001756009.2:n.5277C=
XR_001756010.2:n.5245C=
XR_001756011.2:n.5142C=
XR_001756012.2:n.5290C=
XR_001756013.2:n.4608C=
XR_002958832.1:n.4862C=
XR_002958834.1:n.4933C=
XR_002958835.1:n.4816C=
XR_002958836.1:n.5467C=
XR_002958837.1:n.5274C=
XR_244571.4:n.4794C=
XR_430568.4:n.5313C=
NM_001146706.2:c.4368C=	NP_001140178.1:p.His1456=
NM_004653.5:c.4539C= MANE Select	NP_004644.2:p.His1513=
NM_001146705.2:c.4632C=	NP_001140177.1:p.His1544=