Canonical Allele Identifier: CA520516578
Gene: KDM5D HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21869405A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707519A>G , CM000686.2:g.19707519A>G GRCh38
NC_000024.9:g.21869405A>G , CM000686.1:g.21869405A>G GRCh37
NC_000024.8:g.20328793A>G NCBI36
NG_032920.1:g.42421T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3627T>C MANE Select ENSP00000322408.4:p.Ser1209=
ENST00000317961.8:c.3627T>C ENSP00000322408.4:p.Ser1209=
ENST00000382806.6:c.3456T>C ENSP00000372256.2:p.Ser1152=
ENST00000415360.1:c.543T>C ENSP00000389433.1:p.Ser181=
ENST00000440077.5:c.3504T>C ENSP00000398543.1:p.Ser1168=
ENST00000469599.6:n.2225T>C
ENST00000492117.1:n.3519T>C
ENST00000541639.5:c.3720T>C ENSP00000444293.1:p.Ser1240=
NM_001146705.1:c.3720T>C NP_001140177.1:p.Ser1240=
NM_001146706.1:c.3456T>C NP_001140178.1:p.Ser1152=
NM_004653.4:c.3627T>C NP_004644.2:p.Ser1209=
XM_005262560.1:c.3492T>C XP_005262617.1:p.Ser1164=
XM_005262561.1:c.3396T>C XP_005262618.1:p.Ser1132=
XM_011531468.1:c.3549T>C XP_011529770.1:p.Ser1183=
XR_244571.2:n.3915T>C
XR_430568.2:n.4249T>C
XM_005262560.3:c.3492T>C XP_005262617.1:p.Ser1164=
XM_005262561.3:c.3396T>C XP_005262618.1:p.Ser1132=
XM_011531468.3:c.3549T>C XP_011529770.1:p.Ser1183=
XM_024452495.1:c.1617T>C XP_024308263.1:p.Ser539=
XM_024452496.1:c.1383T>C XP_024308264.1:p.Ser461=
XR_001756009.2:n.4365T>C
XR_001756010.2:n.4365T>C
XR_001756011.2:n.4230T>C
XR_001756012.2:n.4378T>C
XR_001756013.2:n.3696T>C
XR_002958832.1:n.3797T>C
XR_002958834.1:n.4021T>C
XR_002958835.1:n.3904T>C
XR_002958836.1:n.4587T>C
XR_002958837.1:n.4394T>C
XR_244571.4:n.3914T>C
XR_430568.4:n.4248T>C
NM_001146706.2:c.3456T>C NP_001140178.1:p.Ser1152=
NM_004653.5:c.3627T>C MANE Select NP_004644.2:p.Ser1209=
NM_001146705.2:c.3720T>C NP_001140177.1:p.Ser1240=