Canonical Allele Identifier: CA520516535

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869387A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707501A>G , CM000686.2:g.19707501A>G	GRCh38
NC_000024.9:g.21869387A>G , CM000686.1:g.21869387A>G	GRCh37
NC_000024.8:g.20328775A>G	NCBI36
NG_032920.1:g.42439T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3645T>C MANE Select	ENSP00000322408.4:p.Thr1215=
ENST00000317961.8:c.3645T>C	ENSP00000322408.4:p.Thr1215=
ENST00000382806.6:c.3474T>C	ENSP00000372256.2:p.Thr1158=
ENST00000415360.1:c.561T>C	ENSP00000389433.1:p.Thr187=
ENST00000440077.5:c.3522T>C	ENSP00000398543.1:p.Thr1174=
ENST00000469599.6:n.2243T>C
ENST00000492117.1:n.3537T>C
ENST00000541639.5:c.3738T>C	ENSP00000444293.1:p.Thr1246=
NM_001146705.1:c.3738T>C	NP_001140177.1:p.Thr1246=
NM_001146706.1:c.3474T>C	NP_001140178.1:p.Thr1158=
NM_004653.4:c.3645T>C	NP_004644.2:p.Thr1215=
XM_005262560.1:c.3510T>C	XP_005262617.1:p.Thr1170=
XM_005262561.1:c.3414T>C	XP_005262618.1:p.Thr1138=
XM_011531468.1:c.3567T>C	XP_011529770.1:p.Thr1189=
XR_244571.2:n.3933T>C
XR_430568.2:n.4267T>C
XM_005262560.3:c.3510T>C	XP_005262617.1:p.Thr1170=
XM_005262561.3:c.3414T>C	XP_005262618.1:p.Thr1138=
XM_011531468.3:c.3567T>C	XP_011529770.1:p.Thr1189=
XM_024452495.1:c.1635T>C	XP_024308263.1:p.Thr545=
XM_024452496.1:c.1401T>C	XP_024308264.1:p.Thr467=
XR_001756009.2:n.4383T>C
XR_001756010.2:n.4383T>C
XR_001756011.2:n.4248T>C
XR_001756012.2:n.4396T>C
XR_001756013.2:n.3714T>C
XR_002958832.1:n.3815T>C
XR_002958834.1:n.4039T>C
XR_002958835.1:n.3922T>C
XR_002958836.1:n.4605T>C
XR_002958837.1:n.4412T>C
XR_244571.4:n.3932T>C
XR_430568.4:n.4266T>C
NM_001146706.2:c.3474T>C	NP_001140178.1:p.Thr1158=
NM_004653.5:c.3645T>C MANE Select	NP_004644.2:p.Thr1215=
NM_001146705.2:c.3738T>C	NP_001140177.1:p.Thr1246=