Canonical Allele Identifier: CA2470918977

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707689G= , CM000686.2:g.19707689G=	GRCh38
NC_000024.9:g.21869575G= , CM000686.1:g.21869575G=	GRCh37
NC_000024.8:g.20328963G=	NCBI36
NG_032920.1:g.42251C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3457C= MANE Select	ENSP00000322408.4:p.Arg1153=
ENST00000317961.8:c.3457C=	ENSP00000322408.4:p.Arg1153=
ENST00000382806.6:c.3286C=	ENSP00000372256.2:p.Arg1096=
ENST00000415360.1:c.373C=	ENSP00000389433.1:p.Arg125=
ENST00000440077.5:c.3334C=	ENSP00000398543.1:p.Arg1112=
ENST00000469599.6:n.2055C=
ENST00000492117.1:n.3349C=
ENST00000541639.5:c.3550C=	ENSP00000444293.1:p.Arg1184=
NM_001146705.1:c.3550C=	NP_001140177.1:p.Arg1184=
NM_001146706.1:c.3286C=	NP_001140178.1:p.Arg1096=
NM_004653.4:c.3457C=	NP_004644.2:p.Arg1153=
XM_005262560.1:c.3322C=	XP_005262617.1:p.Arg1108=
XM_005262561.1:c.3226C=	XP_005262618.1:p.Arg1076=
XM_011531468.1:c.3379C=	XP_011529770.1:p.Arg1127=
XR_244571.2:n.3745C=
XR_430568.2:n.4079C=
XM_005262560.3:c.3322C=	XP_005262617.1:p.Arg1108=
XM_005262561.3:c.3226C=	XP_005262618.1:p.Arg1076=
XM_011531468.3:c.3379C=	XP_011529770.1:p.Arg1127=
XM_024452495.1:c.1447C=	XP_024308263.1:p.Arg483=
XM_024452496.1:c.1213C=	XP_024308264.1:p.Arg405=
XR_001756009.2:n.4195C=
XR_001756010.2:n.4195C=
XR_001756011.2:n.4060C=
XR_001756012.2:n.4208C=
XR_001756013.2:n.3526C=
XR_002958832.1:n.3627C=
XR_002958834.1:n.3851C=
XR_002958835.1:n.3734C=
XR_002958836.1:n.4417C=
XR_002958837.1:n.4224C=
XR_244571.4:n.3744C=
XR_430568.4:n.4078C=
NM_001146706.2:c.3286C=	NP_001140178.1:p.Arg1096=
NM_004653.5:c.3457C= MANE Select	NP_004644.2:p.Arg1153=
NM_001146705.2:c.3550C=	NP_001140177.1:p.Arg1184=