Canonical Allele Identifier: CA520159509
Gene: KDM5D HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21868010G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19706124G>T , CM000686.2:g.19706124G>T GRCh38
NC_000024.9:g.21868010G>T , CM000686.1:g.21868010G>T GRCh37
NC_000024.8:g.20327398G>T NCBI36
NG_032920.1:g.43816C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.4491C>A MANE Select ENSP00000322408.4:p.Ser1497=
ENST00000317961.8:c.4491C>A ENSP00000322408.4:p.Ser1497=
ENST00000382806.6:c.4320C>A ENSP00000372256.2:p.Ser1440=
ENST00000440077.5:c.4368C>A ENSP00000398543.1:p.Ser1456=
ENST00000469599.6:n.3242C>A
ENST00000492117.1:n.4536C>A
ENST00000541639.5:c.4584C>A ENSP00000444293.1:p.Ser1528=
NM_001146705.1:c.4584C>A NP_001140177.1:p.Ser1528=
NM_001146706.1:c.4320C>A NP_001140178.1:p.Ser1440=
NM_004653.4:c.4491C>A NP_004644.2:p.Ser1497=
XM_005262560.1:c.4356C>A XP_005262617.1:p.Ser1452=
XM_005262561.1:c.4260C>A XP_005262618.1:p.Ser1420=
XM_011531468.1:c.4413C>A XP_011529770.1:p.Ser1471=
XR_430568.2:n.5266C>A
XM_005262560.3:c.4356C>A XP_005262617.1:p.Ser1452=
XM_005262561.3:c.4260C>A XP_005262618.1:p.Ser1420=
XM_011531468.3:c.4413C>A XP_011529770.1:p.Ser1471=
XM_024452495.1:c.2481C>A XP_024308263.1:p.Ser827=
XM_024452496.1:c.2247C>A XP_024308264.1:p.Ser749=
XR_001756009.2:n.5229C>A
XR_001756010.2:n.5197C>A
XR_001756011.2:n.5094C>A
XR_001756012.2:n.5242C>A
XR_001756013.2:n.4560C>A
XR_002958832.1:n.4814C>A
XR_002958834.1:n.4885C>A
XR_002958835.1:n.4768C>A
XR_002958836.1:n.5419C>A
XR_002958837.1:n.5226C>A
XR_244571.4:n.4746C>A
XR_430568.4:n.5265C>A
NM_001146706.2:c.4320C>A NP_001140178.1:p.Ser1440=
NM_004653.5:c.4491C>A MANE Select NP_004644.2:p.Ser1497=
NM_001146705.2:c.4584C>A NP_001140177.1:p.Ser1528=