Canonical Allele Identifier: CA520159149
Gene: KDM5D HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21867882C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19705996C>T , CM000686.2:g.19705996C>T GRCh38
NC_000024.9:g.21867882C>T , CM000686.1:g.21867882C>T GRCh37
NC_000024.8:g.20327270C>T NCBI36
NG_032920.1:g.43944G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000317961.9:c.4619G>A MANE Select ENSP00000322408.4:p.Ter1540=
ENST00000317961.8:c.4619G>A ENSP00000322408.4:p.Ter1540=
ENST00000382806.6:c.4448G>A ENSP00000372256.2:p.Ter1483=
ENST00000469599.6:n.3370G>A
ENST00000492117.1:n.4664G>A
ENST00000541639.5:c.4712G>A ENSP00000444293.1:p.Ter1571=
NM_001146705.1:c.4712G>A NP_001140177.1:p.Ter1571=
NM_001146706.1:c.4448G>A NP_001140178.1:p.Ter1483=
NM_004653.4:c.4619G>A NP_004644.2:p.Ter1540=
XM_005262560.1:c.4484G>A XP_005262617.1:p.Ter1495=
XM_005262561.1:c.4388G>A XP_005262618.1:p.Ter1463=
XM_011531468.1:c.4541G>A XP_011529770.1:p.Ter1514=
XR_430568.2:n.5394G>A
XM_005262560.3:c.4484G>A XP_005262617.1:p.Ter1495=
XM_005262561.3:c.4388G>A XP_005262618.1:p.Ter1463=
XM_011531468.3:c.4541G>A XP_011529770.1:p.Ter1514=
XM_024452495.1:c.2609G>A XP_024308263.1:p.Ter870=
XM_024452496.1:c.2375G>A XP_024308264.1:p.Ter792=
XR_001756009.2:n.5357G>A
XR_001756010.2:n.5325G>A
XR_001756011.2:n.5222G>A
XR_001756012.2:n.5370G>A
XR_001756013.2:n.4688G>A
XR_002958832.1:n.4942G>A
XR_002958834.1:n.5013G>A
XR_002958835.1:n.4896G>A
XR_002958836.1:n.5547G>A
XR_002958837.1:n.5354G>A
XR_244571.4:n.4874G>A
XR_430568.4:n.5393G>A
NM_001146706.2:c.4448G>A NP_001140178.1:p.Ter1483=
NM_004653.5:c.4619G>A MANE Select NP_004644.2:p.Ter1540=
NM_001146705.2:c.4712G>A NP_001140177.1:p.Ter1571=