Canonical Allele Identifier: CA520159387

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21867965T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706079T>C , CM000686.2:g.19706079T>C	GRCh38
NC_000024.9:g.21867965T>C , CM000686.1:g.21867965T>C	GRCh37
NC_000024.8:g.20327353T>C	NCBI36
NG_032920.1:g.43861A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4536A>G MANE Select	ENSP00000322408.4:p.Gln1512=
ENST00000317961.8:c.4536A>G	ENSP00000322408.4:p.Gln1512=
ENST00000382806.6:c.4365A>G	ENSP00000372256.2:p.Gln1455=
ENST00000440077.5:c.4413A>G	ENSP00000398543.1:p.Gln1471=
ENST00000469599.6:n.3287A>G
ENST00000492117.1:n.4581A>G
ENST00000541639.5:c.4629A>G	ENSP00000444293.1:p.Gln1543=
NM_001146705.1:c.4629A>G	NP_001140177.1:p.Gln1543=
NM_001146706.1:c.4365A>G	NP_001140178.1:p.Gln1455=
NM_004653.4:c.4536A>G	NP_004644.2:p.Gln1512=
XM_005262560.1:c.4401A>G	XP_005262617.1:p.Gln1467=
XM_005262561.1:c.4305A>G	XP_005262618.1:p.Gln1435=
XM_011531468.1:c.4458A>G	XP_011529770.1:p.Gln1486=
XR_430568.2:n.5311A>G
XM_005262560.3:c.4401A>G	XP_005262617.1:p.Gln1467=
XM_005262561.3:c.4305A>G	XP_005262618.1:p.Gln1435=
XM_011531468.3:c.4458A>G	XP_011529770.1:p.Gln1486=
XM_024452495.1:c.2526A>G	XP_024308263.1:p.Gln842=
XM_024452496.1:c.2292A>G	XP_024308264.1:p.Gln764=
XR_001756009.2:n.5274A>G
XR_001756010.2:n.5242A>G
XR_001756011.2:n.5139A>G
XR_001756012.2:n.5287A>G
XR_001756013.2:n.4605A>G
XR_002958832.1:n.4859A>G
XR_002958834.1:n.4930A>G
XR_002958835.1:n.4813A>G
XR_002958836.1:n.5464A>G
XR_002958837.1:n.5271A>G
XR_244571.4:n.4791A>G
XR_430568.4:n.5310A>G
NM_001146706.2:c.4365A>G	NP_001140178.1:p.Gln1455=
NM_004653.5:c.4536A>G MANE Select	NP_004644.2:p.Gln1512=
NM_001146705.2:c.4629A>G	NP_001140177.1:p.Gln1543=