Canonical Allele Identifier: CA2470918771

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706094G= , CM000686.2:g.19706094G=	GRCh38
NC_000024.9:g.21867980G= , CM000686.1:g.21867980G=	GRCh37
NC_000024.8:g.20327368G=	NCBI36
NG_032920.1:g.43846C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4521C= MANE Select	ENSP00000322408.4:p.Asn1507=
ENST00000317961.8:c.4521C=	ENSP00000322408.4:p.Asn1507=
ENST00000382806.6:c.4350C=	ENSP00000372256.2:p.Asn1450=
ENST00000440077.5:c.4398C=	ENSP00000398543.1:p.Asn1466=
ENST00000469599.6:n.3272C=
ENST00000492117.1:n.4566C=
ENST00000541639.5:c.4614C=	ENSP00000444293.1:p.Asn1538=
NM_001146705.1:c.4614C=	NP_001140177.1:p.Asn1538=
NM_001146706.1:c.4350C=	NP_001140178.1:p.Asn1450=
NM_004653.4:c.4521C=	NP_004644.2:p.Asn1507=
XM_005262560.1:c.4386C=	XP_005262617.1:p.Asn1462=
XM_005262561.1:c.4290C=	XP_005262618.1:p.Asn1430=
XM_011531468.1:c.4443C=	XP_011529770.1:p.Asn1481=
XR_430568.2:n.5296C=
XM_005262560.3:c.4386C=	XP_005262617.1:p.Asn1462=
XM_005262561.3:c.4290C=	XP_005262618.1:p.Asn1430=
XM_011531468.3:c.4443C=	XP_011529770.1:p.Asn1481=
XM_024452495.1:c.2511C=	XP_024308263.1:p.Asn837=
XM_024452496.1:c.2277C=	XP_024308264.1:p.Asn759=
XR_001756009.2:n.5259C=
XR_001756010.2:n.5227C=
XR_001756011.2:n.5124C=
XR_001756012.2:n.5272C=
XR_001756013.2:n.4590C=
XR_002958832.1:n.4844C=
XR_002958834.1:n.4915C=
XR_002958835.1:n.4798C=
XR_002958836.1:n.5449C=
XR_002958837.1:n.5256C=
XR_244571.4:n.4776C=
XR_430568.4:n.5295C=
NM_001146706.2:c.4350C=	NP_001140178.1:p.Asn1450=
NM_004653.5:c.4521C= MANE Select	NP_004644.2:p.Asn1507=
NM_001146705.2:c.4614C=	NP_001140177.1:p.Asn1538=