Canonical Allele Identifier: CA520516550
Gene: KDM5D HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21869396G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707510G>T , CM000686.2:g.19707510G>T GRCh38
NC_000024.9:g.21869396G>T , CM000686.1:g.21869396G>T GRCh37
NC_000024.8:g.20328784G>T NCBI36
NG_032920.1:g.42430C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3636C>A MANE Select ENSP00000322408.4:p.Pro1212=
ENST00000317961.8:c.3636C>A ENSP00000322408.4:p.Pro1212=
ENST00000382806.6:c.3465C>A ENSP00000372256.2:p.Pro1155=
ENST00000415360.1:c.552C>A ENSP00000389433.1:p.Pro184=
ENST00000440077.5:c.3513C>A ENSP00000398543.1:p.Pro1171=
ENST00000469599.6:n.2234C>A
ENST00000492117.1:n.3528C>A
ENST00000541639.5:c.3729C>A ENSP00000444293.1:p.Pro1243=
NM_001146705.1:c.3729C>A NP_001140177.1:p.Pro1243=
NM_001146706.1:c.3465C>A NP_001140178.1:p.Pro1155=
NM_004653.4:c.3636C>A NP_004644.2:p.Pro1212=
XM_005262560.1:c.3501C>A XP_005262617.1:p.Pro1167=
XM_005262561.1:c.3405C>A XP_005262618.1:p.Pro1135=
XM_011531468.1:c.3558C>A XP_011529770.1:p.Pro1186=
XR_244571.2:n.3924C>A
XR_430568.2:n.4258C>A
XM_005262560.3:c.3501C>A XP_005262617.1:p.Pro1167=
XM_005262561.3:c.3405C>A XP_005262618.1:p.Pro1135=
XM_011531468.3:c.3558C>A XP_011529770.1:p.Pro1186=
XM_024452495.1:c.1626C>A XP_024308263.1:p.Pro542=
XM_024452496.1:c.1392C>A XP_024308264.1:p.Pro464=
XR_001756009.2:n.4374C>A
XR_001756010.2:n.4374C>A
XR_001756011.2:n.4239C>A
XR_001756012.2:n.4387C>A
XR_001756013.2:n.3705C>A
XR_002958832.1:n.3806C>A
XR_002958834.1:n.4030C>A
XR_002958835.1:n.3913C>A
XR_002958836.1:n.4596C>A
XR_002958837.1:n.4403C>A
XR_244571.4:n.3923C>A
XR_430568.4:n.4257C>A
NM_001146706.2:c.3465C>A NP_001140178.1:p.Pro1155=
NM_004653.5:c.3636C>A MANE Select NP_004644.2:p.Pro1212=
NM_001146705.2:c.3729C>A NP_001140177.1:p.Pro1243=