Canonical Allele Identifier: CA520159472
Gene: KDM5D HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21867998G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19706112G>A , CM000686.2:g.19706112G>A GRCh38
NC_000024.9:g.21867998G>A , CM000686.1:g.21867998G>A GRCh37
NC_000024.8:g.20327386G>A NCBI36
NG_032920.1:g.43828C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.4503C>T MANE Select ENSP00000322408.4:p.Ser1501=
ENST00000317961.8:c.4503C>T ENSP00000322408.4:p.Ser1501=
ENST00000382806.6:c.4332C>T ENSP00000372256.2:p.Ser1444=
ENST00000440077.5:c.4380C>T ENSP00000398543.1:p.Ser1460=
ENST00000469599.6:n.3254C>T
ENST00000492117.1:n.4548C>T
ENST00000541639.5:c.4596C>T ENSP00000444293.1:p.Ser1532=
NM_001146705.1:c.4596C>T NP_001140177.1:p.Ser1532=
NM_001146706.1:c.4332C>T NP_001140178.1:p.Ser1444=
NM_004653.4:c.4503C>T NP_004644.2:p.Ser1501=
XM_005262560.1:c.4368C>T XP_005262617.1:p.Ser1456=
XM_005262561.1:c.4272C>T XP_005262618.1:p.Ser1424=
XM_011531468.1:c.4425C>T XP_011529770.1:p.Ser1475=
XR_430568.2:n.5278C>T
XM_005262560.3:c.4368C>T XP_005262617.1:p.Ser1456=
XM_005262561.3:c.4272C>T XP_005262618.1:p.Ser1424=
XM_011531468.3:c.4425C>T XP_011529770.1:p.Ser1475=
XM_024452495.1:c.2493C>T XP_024308263.1:p.Ser831=
XM_024452496.1:c.2259C>T XP_024308264.1:p.Ser753=
XR_001756009.2:n.5241C>T
XR_001756010.2:n.5209C>T
XR_001756011.2:n.5106C>T
XR_001756012.2:n.5254C>T
XR_001756013.2:n.4572C>T
XR_002958832.1:n.4826C>T
XR_002958834.1:n.4897C>T
XR_002958835.1:n.4780C>T
XR_002958836.1:n.5431C>T
XR_002958837.1:n.5238C>T
XR_244571.4:n.4758C>T
XR_430568.4:n.5277C>T
NM_001146706.2:c.4332C>T NP_001140178.1:p.Ser1444=
NM_004653.5:c.4503C>T MANE Select NP_004644.2:p.Ser1501=
NM_001146705.2:c.4596C>T NP_001140177.1:p.Ser1532=