Canonical Allele Identifier: CA2470920849

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19735435T= , CM000686.2:g.19735435T=	GRCh38
NC_000024.9:g.21897321T= , CM000686.1:g.21897321T=	GRCh37
NC_000024.8:g.20356709T=	NCBI36
NG_032920.1:g.14505A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.850A= MANE Select	ENSP00000322408.4:p.Thr284=
ENST00000317961.8:c.850A=	ENSP00000322408.4:p.Thr284=
ENST00000382806.6:c.679A=	ENSP00000372256.2:p.Thr227=
ENST00000440077.5:c.727A=	ENSP00000398543.1:p.Thr243=
ENST00000447300.1:c.715A=	ENSP00000416377.1:p.Thr239=
ENST00000541639.5:c.850A=	ENSP00000444293.1:p.Thr284=
NM_001146705.1:c.850A=	NP_001140177.1:p.Thr284=
NM_001146706.1:c.679A=	NP_001140178.1:p.Thr227=
NM_004653.4:c.850A=	NP_004644.2:p.Thr284=
XM_005262560.1:c.715A=	XP_005262617.1:p.Thr239=
XM_005262561.1:c.850A=	XP_005262618.1:p.Thr284=
XM_005262562.2:c.850A=	XP_005262619.1:p.Thr284=
XM_011531468.1:c.850A=	XP_011529770.1:p.Thr284=
XR_244571.2:n.1138A=
XR_430568.2:n.1138A=
XR_938609.1:n.1138A=
XR_938610.1:n.1138A=
XM_005262560.3:c.715A=	XP_005262617.1:p.Thr239=
XM_005262561.3:c.850A=	XP_005262618.1:p.Thr284=
XM_011531468.3:c.850A=	XP_011529770.1:p.Thr284=
XM_024452495.1:c.-1268A=	XP_024308263.1:n.-1268A=
XR_001756009.2:n.1137A=
XR_001756010.2:n.1137A=
XR_001756011.2:n.1002A=
XR_001756012.2:n.1137A=
XR_001756013.2:n.1137A=
XR_002958832.1:n.1137A=
XR_002958833.1:n.1137A=
XR_002958834.1:n.1137A=
XR_002958835.1:n.1137A=
XR_002958836.1:n.1137A=
XR_002958837.1:n.1137A=
XR_244571.4:n.1137A=
XR_430568.4:n.1137A=
NM_001146706.2:c.679A=	NP_001140178.1:p.Thr227=
NM_004653.5:c.850A= MANE Select	NP_004644.2:p.Thr284=
NM_001146705.2:c.850A=	NP_001140177.1:p.Thr284=