Canonical Allele Identifier: CA520514730

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21868034A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706148A>C , CM000686.2:g.19706148A>C	GRCh38
NC_000024.9:g.21868034A>C , CM000686.1:g.21868034A>C	GRCh37
NC_000024.8:g.20327422A>C	NCBI36
NG_032920.1:g.43792T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4467T>G MANE Select	ENSP00000322408.4:p.Arg1489=
ENST00000317961.8:c.4467T>G	ENSP00000322408.4:p.Arg1489=
ENST00000382806.6:c.4296T>G	ENSP00000372256.2:p.Arg1432=
ENST00000440077.5:c.4344T>G	ENSP00000398543.1:p.Arg1448=
ENST00000469599.6:n.3218T>G
ENST00000492117.1:n.4512T>G
ENST00000541639.5:c.4560T>G	ENSP00000444293.1:p.Arg1520=
NM_001146705.1:c.4560T>G	NP_001140177.1:p.Arg1520=
NM_001146706.1:c.4296T>G	NP_001140178.1:p.Arg1432=
NM_004653.4:c.4467T>G	NP_004644.2:p.Arg1489=
XM_005262560.1:c.4332T>G	XP_005262617.1:p.Arg1444=
XM_005262561.1:c.4236T>G	XP_005262618.1:p.Arg1412=
XM_011531468.1:c.4389T>G	XP_011529770.1:p.Arg1463=
XR_430568.2:n.5242T>G
XM_005262560.3:c.4332T>G	XP_005262617.1:p.Arg1444=
XM_005262561.3:c.4236T>G	XP_005262618.1:p.Arg1412=
XM_011531468.3:c.4389T>G	XP_011529770.1:p.Arg1463=
XM_024452495.1:c.2457T>G	XP_024308263.1:p.Arg819=
XM_024452496.1:c.2223T>G	XP_024308264.1:p.Arg741=
XR_001756009.2:n.5205T>G
XR_001756010.2:n.5173T>G
XR_001756011.2:n.5070T>G
XR_001756012.2:n.5218T>G
XR_001756013.2:n.4536T>G
XR_002958832.1:n.4790T>G
XR_002958834.1:n.4861T>G
XR_002958835.1:n.4744T>G
XR_002958836.1:n.5395T>G
XR_002958837.1:n.5202T>G
XR_244571.4:n.4722T>G
XR_430568.4:n.5241T>G
NM_001146706.2:c.4296T>G	NP_001140178.1:p.Arg1432=
NM_004653.5:c.4467T>G MANE Select	NP_004644.2:p.Arg1489=
NM_001146705.2:c.4560T>G	NP_001140177.1:p.Arg1520=