Canonical Allele Identifier: CA2470918875

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706840T= , CM000686.2:g.19706840T=	GRCh38
NC_000024.9:g.21868726T= , CM000686.1:g.21868726T=	GRCh37
NC_000024.8:g.20328114T=	NCBI36
NG_032920.1:g.43100A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4023A= MANE Select	ENSP00000322408.4:p.Gly1341=
ENST00000317961.8:c.4023A=	ENSP00000322408.4:p.Gly1341=
ENST00000382806.6:c.3852A=	ENSP00000372256.2:p.Gly1284=
ENST00000440077.5:c.3900A=	ENSP00000398543.1:p.Gly1300=
ENST00000469599.6:n.2621A=
ENST00000492117.1:n.3915A=
ENST00000541639.5:c.4116A=	ENSP00000444293.1:p.Gly1372=
NM_001146705.1:c.4116A=	NP_001140177.1:p.Gly1372=
NM_001146706.1:c.3852A=	NP_001140178.1:p.Gly1284=
NM_004653.4:c.4023A=	NP_004644.2:p.Gly1341=
XM_005262560.1:c.3888A=	XP_005262617.1:p.Gly1296=
XM_005262561.1:c.3792A=	XP_005262618.1:p.Gly1264=
XM_011531468.1:c.3945A=	XP_011529770.1:p.Gly1315=
XR_244571.2:n.4311A=
XR_430568.2:n.4645A=
XM_005262560.3:c.3888A=	XP_005262617.1:p.Gly1296=
XM_005262561.3:c.3792A=	XP_005262618.1:p.Gly1264=
XM_011531468.3:c.3945A=	XP_011529770.1:p.Gly1315=
XM_024452495.1:c.2013A=	XP_024308263.1:p.Gly671=
XM_024452496.1:c.1779A=	XP_024308264.1:p.Gly593=
XR_001756009.2:n.4761A=
XR_001756010.2:n.4761A=
XR_001756011.2:n.4626A=
XR_001756012.2:n.4774A=
XR_001756013.2:n.4092A=
XR_002958832.1:n.4193A=
XR_002958834.1:n.4417A=
XR_002958835.1:n.4300A=
XR_002958836.1:n.4983A=
XR_002958837.1:n.4790A=
XR_244571.4:n.4310A=
XR_430568.4:n.4644A=
NM_001146706.2:c.3852A=	NP_001140178.1:p.Gly1284=
NM_004653.5:c.4023A= MANE Select	NP_004644.2:p.Gly1341=
NM_001146705.2:c.4116A=	NP_001140177.1:p.Gly1372=