Canonical Allele Identifier: CA2470919010

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19708028C= , CM000686.2:g.19708028C=	GRCh38
NC_000024.9:g.21869914C= , CM000686.1:g.21869914C=	GRCh37
NC_000024.8:g.20329302C=	NCBI36
NG_032920.1:g.41912G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3305G= MANE Select	ENSP00000322408.4:p.Arg1102=
ENST00000317961.8:c.3305G=	ENSP00000322408.4:p.Arg1102=
ENST00000382806.6:c.3134G=	ENSP00000372256.2:p.Arg1045=
ENST00000415360.1:c.221G=	ENSP00000389433.1:p.Arg74=
ENST00000440077.5:c.3182G=	ENSP00000398543.1:p.Arg1061=
ENST00000469599.6:n.1903G=
ENST00000492117.1:n.3197G=
ENST00000541639.5:c.3398G=	ENSP00000444293.1:p.Arg1133=
NM_001146705.1:c.3398G=	NP_001140177.1:p.Arg1133=
NM_001146706.1:c.3134G=	NP_001140178.1:p.Arg1045=
NM_004653.4:c.3305G=	NP_004644.2:p.Arg1102=
XM_005262560.1:c.3170G=	XP_005262617.1:p.Arg1057=
XM_005262561.1:c.3074G=	XP_005262618.1:p.Arg1025=
XM_011531468.1:c.3227G=	XP_011529770.1:p.Arg1076=
XR_244571.2:n.3593G=
XR_430568.2:n.3927G=
XM_005262560.3:c.3170G=	XP_005262617.1:p.Arg1057=
XM_005262561.3:c.3074G=	XP_005262618.1:p.Arg1025=
XM_011531468.3:c.3227G=	XP_011529770.1:p.Arg1076=
XM_024452495.1:c.1295G=	XP_024308263.1:p.Arg432=
XM_024452496.1:c.1061G=	XP_024308264.1:p.Arg354=
XR_001756009.2:n.4043G=
XR_001756010.2:n.4043G=
XR_001756011.2:n.3908G=
XR_001756012.2:n.4056G=
XR_001756013.2:n.3374G=
XR_002958832.1:n.3475G=
XR_002958834.1:n.3699G=
XR_002958835.1:n.3582G=
XR_002958836.1:n.4265G=
XR_002958837.1:n.4072G=
XR_244571.4:n.3592G=
XR_430568.4:n.3926G=
NM_001146706.2:c.3134G=	NP_001140178.1:p.Arg1045=
NM_004653.5:c.3305G= MANE Select	NP_004644.2:p.Arg1102=
NM_001146705.2:c.3398G=	NP_001140177.1:p.Arg1133=