Canonical Allele Identifier: CA520159887

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21868684G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706798G>C , CM000686.2:g.19706798G>C	GRCh38
NC_000024.9:g.21868684G>C , CM000686.1:g.21868684G>C	GRCh37
NC_000024.8:g.20328072G>C	NCBI36
NG_032920.1:g.43142C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000317961.9:c.4065C>G MANE Select	ENSP00000322408.4:p.Gly1355=
ENST00000317961.8:c.4065C>G	ENSP00000322408.4:p.Gly1355=
ENST00000382806.6:c.3894C>G	ENSP00000372256.2:p.Gly1298=
ENST00000440077.5:c.3942C>G	ENSP00000398543.1:p.Gly1314=
ENST00000469599.6:n.2663C>G
ENST00000492117.1:n.3957C>G
ENST00000541639.5:c.4158C>G	ENSP00000444293.1:p.Gly1386=
NM_001146705.1:c.4158C>G	NP_001140177.1:p.Gly1386=
NM_001146706.1:c.3894C>G	NP_001140178.1:p.Gly1298=
NM_004653.4:c.4065C>G	NP_004644.2:p.Gly1355=
XM_005262560.1:c.3930C>G	XP_005262617.1:p.Gly1310=
XM_005262561.1:c.3834C>G	XP_005262618.1:p.Gly1278=
XM_011531468.1:c.3987C>G	XP_011529770.1:p.Gly1329=
XR_244571.2:n.4353C>G
XR_430568.2:n.4687C>G
XM_005262560.3:c.3930C>G	XP_005262617.1:p.Gly1310=
XM_005262561.3:c.3834C>G	XP_005262618.1:p.Gly1278=
XM_011531468.3:c.3987C>G	XP_011529770.1:p.Gly1329=
XM_024452495.1:c.2055C>G	XP_024308263.1:p.Gly685=
XM_024452496.1:c.1821C>G	XP_024308264.1:p.Gly607=
XR_001756009.2:n.4803C>G
XR_001756010.2:n.4803C>G
XR_001756011.2:n.4668C>G
XR_001756012.2:n.4816C>G
XR_001756013.2:n.4134C>G
XR_002958832.1:n.4235C>G
XR_002958834.1:n.4459C>G
XR_002958835.1:n.4342C>G
XR_002958836.1:n.5025C>G
XR_002958837.1:n.4832C>G
XR_244571.4:n.4352C>G
XR_430568.4:n.4686C>G
NM_001146706.2:c.3894C>G	NP_001140178.1:p.Gly1298=
NM_004653.5:c.4065C>G MANE Select	NP_004644.2:p.Gly1355=
NM_001146705.2:c.4158C>G	NP_001140177.1:p.Gly1386=