Canonical Allele Identifier: CA2470918767

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706055A= , CM000686.2:g.19706055A=	GRCh38
NC_000024.9:g.21867941A= , CM000686.1:g.21867941A=	GRCh37
NC_000024.8:g.20327329A=	NCBI36
NG_032920.1:g.43885T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4560T= MANE Select	ENSP00000322408.4:p.Ala1520=
ENST00000317961.8:c.4560T=	ENSP00000322408.4:p.Ala1520=
ENST00000382806.6:c.4389T=	ENSP00000372256.2:p.Ala1463=
ENST00000469599.6:n.3311T=
ENST00000492117.1:n.4605T=
ENST00000541639.5:c.4653T=	ENSP00000444293.1:p.Ala1551=
NM_001146705.1:c.4653T=	NP_001140177.1:p.Ala1551=
NM_001146706.1:c.4389T=	NP_001140178.1:p.Ala1463=
NM_004653.4:c.4560T=	NP_004644.2:p.Ala1520=
XM_005262560.1:c.4425T=	XP_005262617.1:p.Ala1475=
XM_005262561.1:c.4329T=	XP_005262618.1:p.Ala1443=
XM_011531468.1:c.4482T=	XP_011529770.1:p.Ala1494=
XR_430568.2:n.5335T=
XM_005262560.3:c.4425T=	XP_005262617.1:p.Ala1475=
XM_005262561.3:c.4329T=	XP_005262618.1:p.Ala1443=
XM_011531468.3:c.4482T=	XP_011529770.1:p.Ala1494=
XM_024452495.1:c.2550T=	XP_024308263.1:p.Ala850=
XM_024452496.1:c.2316T=	XP_024308264.1:p.Ala772=
XR_001756009.2:n.5298T=
XR_001756010.2:n.5266T=
XR_001756011.2:n.5163T=
XR_001756012.2:n.5311T=
XR_001756013.2:n.4629T=
XR_002958832.1:n.4883T=
XR_002958834.1:n.4954T=
XR_002958835.1:n.4837T=
XR_002958836.1:n.5488T=
XR_002958837.1:n.5295T=
XR_244571.4:n.4815T=
XR_430568.4:n.5334T=
NM_001146706.2:c.4389T=	NP_001140178.1:p.Ala1463=
NM_004653.5:c.4560T= MANE Select	NP_004644.2:p.Ala1520=
NM_001146705.2:c.4653T=	NP_001140177.1:p.Ala1551=