Canonical Allele Identifier: CA520516710
Gene: KDM5D HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21869450G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707564G>A , CM000686.2:g.19707564G>A GRCh38
NC_000024.9:g.21869450G>A , CM000686.1:g.21869450G>A GRCh37
NC_000024.8:g.20328838G>A NCBI36
NG_032920.1:g.42376C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3582C>T MANE Select ENSP00000322408.4:p.Asp1194=
ENST00000317961.8:c.3582C>T ENSP00000322408.4:p.Asp1194=
ENST00000382806.6:c.3411C>T ENSP00000372256.2:p.Asp1137=
ENST00000415360.1:c.498C>T ENSP00000389433.1:p.Asp166=
ENST00000440077.5:c.3459C>T ENSP00000398543.1:p.Asp1153=
ENST00000469599.6:n.2180C>T
ENST00000492117.1:n.3474C>T
ENST00000541639.5:c.3675C>T ENSP00000444293.1:p.Asp1225=
NM_001146705.1:c.3675C>T NP_001140177.1:p.Asp1225=
NM_001146706.1:c.3411C>T NP_001140178.1:p.Asp1137=
NM_004653.4:c.3582C>T NP_004644.2:p.Asp1194=
XM_005262560.1:c.3447C>T XP_005262617.1:p.Asp1149=
XM_005262561.1:c.3351C>T XP_005262618.1:p.Asp1117=
XM_011531468.1:c.3504C>T XP_011529770.1:p.Asp1168=
XR_244571.2:n.3870C>T
XR_430568.2:n.4204C>T
XM_005262560.3:c.3447C>T XP_005262617.1:p.Asp1149=
XM_005262561.3:c.3351C>T XP_005262618.1:p.Asp1117=
XM_011531468.3:c.3504C>T XP_011529770.1:p.Asp1168=
XM_024452495.1:c.1572C>T XP_024308263.1:p.Asp524=
XM_024452496.1:c.1338C>T XP_024308264.1:p.Asp446=
XR_001756009.2:n.4320C>T
XR_001756010.2:n.4320C>T
XR_001756011.2:n.4185C>T
XR_001756012.2:n.4333C>T
XR_001756013.2:n.3651C>T
XR_002958832.1:n.3752C>T
XR_002958834.1:n.3976C>T
XR_002958835.1:n.3859C>T
XR_002958836.1:n.4542C>T
XR_002958837.1:n.4349C>T
XR_244571.4:n.3869C>T
XR_430568.4:n.4203C>T
NM_001146706.2:c.3411C>T NP_001140178.1:p.Asp1137=
NM_004653.5:c.3582C>T MANE Select NP_004644.2:p.Asp1194=
NM_001146705.2:c.3675C>T NP_001140177.1:p.Asp1225=