Canonical Allele Identifier: CA2470918772

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706106G= , CM000686.2:g.19706106G=	GRCh38
NC_000024.9:g.21867992G= , CM000686.1:g.21867992G=	GRCh37
NC_000024.8:g.20327380G=	NCBI36
NG_032920.1:g.43834C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4509C= MANE Select	ENSP00000322408.4:p.Phe1503=
ENST00000317961.8:c.4509C=	ENSP00000322408.4:p.Phe1503=
ENST00000382806.6:c.4338C=	ENSP00000372256.2:p.Phe1446=
ENST00000440077.5:c.4386C=	ENSP00000398543.1:p.Phe1462=
ENST00000469599.6:n.3260C=
ENST00000492117.1:n.4554C=
ENST00000541639.5:c.4602C=	ENSP00000444293.1:p.Phe1534=
NM_001146705.1:c.4602C=	NP_001140177.1:p.Phe1534=
NM_001146706.1:c.4338C=	NP_001140178.1:p.Phe1446=
NM_004653.4:c.4509C=	NP_004644.2:p.Phe1503=
XM_005262560.1:c.4374C=	XP_005262617.1:p.Phe1458=
XM_005262561.1:c.4278C=	XP_005262618.1:p.Phe1426=
XM_011531468.1:c.4431C=	XP_011529770.1:p.Phe1477=
XR_430568.2:n.5284C=
XM_005262560.3:c.4374C=	XP_005262617.1:p.Phe1458=
XM_005262561.3:c.4278C=	XP_005262618.1:p.Phe1426=
XM_011531468.3:c.4431C=	XP_011529770.1:p.Phe1477=
XM_024452495.1:c.2499C=	XP_024308263.1:p.Phe833=
XM_024452496.1:c.2265C=	XP_024308264.1:p.Phe755=
XR_001756009.2:n.5247C=
XR_001756010.2:n.5215C=
XR_001756011.2:n.5112C=
XR_001756012.2:n.5260C=
XR_001756013.2:n.4578C=
XR_002958832.1:n.4832C=
XR_002958834.1:n.4903C=
XR_002958835.1:n.4786C=
XR_002958836.1:n.5437C=
XR_002958837.1:n.5244C=
XR_244571.4:n.4764C=
XR_430568.4:n.5283C=
NM_001146706.2:c.4338C=	NP_001140178.1:p.Phe1446=
NM_004653.5:c.4509C= MANE Select	NP_004644.2:p.Phe1503=
NM_001146705.2:c.4602C=	NP_001140177.1:p.Phe1534=