Canonical Allele Identifier: CA2470918761

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706001C= , CM000686.2:g.19706001C=	GRCh38
NC_000024.9:g.21867887C= , CM000686.1:g.21867887C=	GRCh37
NC_000024.8:g.20327275C=	NCBI36
NG_032920.1:g.43939G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4614G= MANE Select	ENSP00000322408.4:p.Gln1538=
ENST00000317961.8:c.4614G=	ENSP00000322408.4:p.Gln1538=
ENST00000382806.6:c.4443G=	ENSP00000372256.2:p.Gln1481=
ENST00000469599.6:n.3365G=
ENST00000492117.1:n.4659G=
ENST00000541639.5:c.4707G=	ENSP00000444293.1:p.Gln1569=
NM_001146705.1:c.4707G=	NP_001140177.1:p.Gln1569=
NM_001146706.1:c.4443G=	NP_001140178.1:p.Gln1481=
NM_004653.4:c.4614G=	NP_004644.2:p.Gln1538=
XM_005262560.1:c.4479G=	XP_005262617.1:p.Gln1493=
XM_005262561.1:c.4383G=	XP_005262618.1:p.Gln1461=
XM_011531468.1:c.4536G=	XP_011529770.1:p.Gln1512=
XR_430568.2:n.5389G=
XM_005262560.3:c.4479G=	XP_005262617.1:p.Gln1493=
XM_005262561.3:c.4383G=	XP_005262618.1:p.Gln1461=
XM_011531468.3:c.4536G=	XP_011529770.1:p.Gln1512=
XM_024452495.1:c.2604G=	XP_024308263.1:p.Gln868=
XM_024452496.1:c.2370G=	XP_024308264.1:p.Gln790=
XR_001756009.2:n.5352G=
XR_001756010.2:n.5320G=
XR_001756011.2:n.5217G=
XR_001756012.2:n.5365G=
XR_001756013.2:n.4683G=
XR_002958832.1:n.4937G=
XR_002958834.1:n.5008G=
XR_002958835.1:n.4891G=
XR_002958836.1:n.5542G=
XR_002958837.1:n.5349G=
XR_244571.4:n.4869G=
XR_430568.4:n.5388G=
NM_001146706.2:c.4443G=	NP_001140178.1:p.Gln1481=
NM_004653.5:c.4614G= MANE Select	NP_004644.2:p.Gln1538=
NM_001146705.2:c.4707G=	NP_001140177.1:p.Gln1569=