Canonical Allele Identifier: CA2470919003

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707972C= , CM000686.2:g.19707972C=	GRCh38
NC_000024.9:g.21869858C= , CM000686.1:g.21869858C=	GRCh37
NC_000024.8:g.20329246C=	NCBI36
NG_032920.1:g.41968G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3361G= MANE Select	ENSP00000322408.4:p.Gly1121=
ENST00000317961.8:c.3361G=	ENSP00000322408.4:p.Gly1121=
ENST00000382806.6:c.3190G=	ENSP00000372256.2:p.Gly1064=
ENST00000415360.1:c.277G=	ENSP00000389433.1:p.Gly93=
ENST00000440077.5:c.3238G=	ENSP00000398543.1:p.Gly1080=
ENST00000469599.6:n.1959G=
ENST00000492117.1:n.3253G=
ENST00000541639.5:c.3454G=	ENSP00000444293.1:p.Gly1152=
NM_001146705.1:c.3454G=	NP_001140177.1:p.Gly1152=
NM_001146706.1:c.3190G=	NP_001140178.1:p.Gly1064=
NM_004653.4:c.3361G=	NP_004644.2:p.Gly1121=
XM_005262560.1:c.3226G=	XP_005262617.1:p.Gly1076=
XM_005262561.1:c.3130G=	XP_005262618.1:p.Gly1044=
XM_011531468.1:c.3283G=	XP_011529770.1:p.Gly1095=
XR_244571.2:n.3649G=
XR_430568.2:n.3983G=
XM_005262560.3:c.3226G=	XP_005262617.1:p.Gly1076=
XM_005262561.3:c.3130G=	XP_005262618.1:p.Gly1044=
XM_011531468.3:c.3283G=	XP_011529770.1:p.Gly1095=
XM_024452495.1:c.1351G=	XP_024308263.1:p.Gly451=
XM_024452496.1:c.1117G=	XP_024308264.1:p.Gly373=
XR_001756009.2:n.4099G=
XR_001756010.2:n.4099G=
XR_001756011.2:n.3964G=
XR_001756012.2:n.4112G=
XR_001756013.2:n.3430G=
XR_002958832.1:n.3531G=
XR_002958834.1:n.3755G=
XR_002958835.1:n.3638G=
XR_002958836.1:n.4321G=
XR_002958837.1:n.4128G=
XR_244571.4:n.3648G=
XR_430568.4:n.3982G=
NM_001146706.2:c.3190G=	NP_001140178.1:p.Gly1064=
NM_004653.5:c.3361G= MANE Select	NP_004644.2:p.Gly1121=
NM_001146705.2:c.3454G=	NP_001140177.1:p.Gly1152=