Canonical Allele Identifier: CA520159355
Gene: KDM5D HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21867953T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19706067T>A , CM000686.2:g.19706067T>A GRCh38
NC_000024.9:g.21867953T>A , CM000686.1:g.21867953T>A GRCh37
NC_000024.8:g.20327341T>A NCBI36
NG_032920.1:g.43873A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.4548A>T MANE Select ENSP00000322408.4:p.Ser1516=
ENST00000317961.8:c.4548A>T ENSP00000322408.4:p.Ser1516=
ENST00000382806.6:c.4377A>T ENSP00000372256.2:p.Ser1459=
ENST00000440077.5:c.4425A>T ENSP00000398543.1:p.Ser1475=
ENST00000469599.6:n.3299A>T
ENST00000492117.1:n.4593A>T
ENST00000541639.5:c.4641A>T ENSP00000444293.1:p.Ser1547=
NM_001146705.1:c.4641A>T NP_001140177.1:p.Ser1547=
NM_001146706.1:c.4377A>T NP_001140178.1:p.Ser1459=
NM_004653.4:c.4548A>T NP_004644.2:p.Ser1516=
XM_005262560.1:c.4413A>T XP_005262617.1:p.Ser1471=
XM_005262561.1:c.4317A>T XP_005262618.1:p.Ser1439=
XM_011531468.1:c.4470A>T XP_011529770.1:p.Ser1490=
XR_430568.2:n.5323A>T
XM_005262560.3:c.4413A>T XP_005262617.1:p.Ser1471=
XM_005262561.3:c.4317A>T XP_005262618.1:p.Ser1439=
XM_011531468.3:c.4470A>T XP_011529770.1:p.Ser1490=
XM_024452495.1:c.2538A>T XP_024308263.1:p.Ser846=
XM_024452496.1:c.2304A>T XP_024308264.1:p.Ser768=
XR_001756009.2:n.5286A>T
XR_001756010.2:n.5254A>T
XR_001756011.2:n.5151A>T
XR_001756012.2:n.5299A>T
XR_001756013.2:n.4617A>T
XR_002958832.1:n.4871A>T
XR_002958834.1:n.4942A>T
XR_002958835.1:n.4825A>T
XR_002958836.1:n.5476A>T
XR_002958837.1:n.5283A>T
XR_244571.4:n.4803A>T
XR_430568.4:n.5322A>T
NM_001146706.2:c.4377A>T NP_001140178.1:p.Ser1459=
NM_004653.5:c.4548A>T MANE Select NP_004644.2:p.Ser1516=
NM_001146705.2:c.4641A>T NP_001140177.1:p.Ser1547=