Canonical Allele Identifier: CA520516644
Gene: KDM5D HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21869429C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707543C>T , CM000686.2:g.19707543C>T GRCh38
NC_000024.9:g.21869429C>T , CM000686.1:g.21869429C>T GRCh37
NC_000024.8:g.20328817C>T NCBI36
NG_032920.1:g.42397G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3603G>A MANE Select ENSP00000322408.4:p.Val1201=
ENST00000317961.8:c.3603G>A ENSP00000322408.4:p.Val1201=
ENST00000382806.6:c.3432G>A ENSP00000372256.2:p.Val1144=
ENST00000415360.1:c.519G>A ENSP00000389433.1:p.Val173=
ENST00000440077.5:c.3480G>A ENSP00000398543.1:p.Val1160=
ENST00000469599.6:n.2201G>A
ENST00000492117.1:n.3495G>A
ENST00000541639.5:c.3696G>A ENSP00000444293.1:p.Val1232=
NM_001146705.1:c.3696G>A NP_001140177.1:p.Val1232=
NM_001146706.1:c.3432G>A NP_001140178.1:p.Val1144=
NM_004653.4:c.3603G>A NP_004644.2:p.Val1201=
XM_005262560.1:c.3468G>A XP_005262617.1:p.Val1156=
XM_005262561.1:c.3372G>A XP_005262618.1:p.Val1124=
XM_011531468.1:c.3525G>A XP_011529770.1:p.Val1175=
XR_244571.2:n.3891G>A
XR_430568.2:n.4225G>A
XM_005262560.3:c.3468G>A XP_005262617.1:p.Val1156=
XM_005262561.3:c.3372G>A XP_005262618.1:p.Val1124=
XM_011531468.3:c.3525G>A XP_011529770.1:p.Val1175=
XM_024452495.1:c.1593G>A XP_024308263.1:p.Val531=
XM_024452496.1:c.1359G>A XP_024308264.1:p.Val453=
XR_001756009.2:n.4341G>A
XR_001756010.2:n.4341G>A
XR_001756011.2:n.4206G>A
XR_001756012.2:n.4354G>A
XR_001756013.2:n.3672G>A
XR_002958832.1:n.3773G>A
XR_002958834.1:n.3997G>A
XR_002958835.1:n.3880G>A
XR_002958836.1:n.4563G>A
XR_002958837.1:n.4370G>A
XR_244571.4:n.3890G>A
XR_430568.4:n.4224G>A
NM_001146706.2:c.3432G>A NP_001140178.1:p.Val1144=
NM_004653.5:c.3603G>A MANE Select NP_004644.2:p.Val1201=
NM_001146705.2:c.3696G>A NP_001140177.1:p.Val1232=