Canonical Allele Identifier: CA520160807
Gene: KDM5D HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21869829T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707943T>A , CM000686.2:g.19707943T>A GRCh38
NC_000024.9:g.21869829T>A , CM000686.1:g.21869829T>A GRCh37
NC_000024.8:g.20329217T>A NCBI36
NG_032920.1:g.41997A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000317961.9:c.3390A>T MANE Select ENSP00000322408.4:p.Pro1130=
ENST00000317961.8:c.3390A>T ENSP00000322408.4:p.Pro1130=
ENST00000382806.6:c.3219A>T ENSP00000372256.2:p.Pro1073=
ENST00000415360.1:c.306A>T ENSP00000389433.1:p.Pro102=
ENST00000440077.5:c.3267A>T ENSP00000398543.1:p.Pro1089=
ENST00000469599.6:n.1988A>T
ENST00000492117.1:n.3282A>T
ENST00000541639.5:c.3483A>T ENSP00000444293.1:p.Pro1161=
NM_001146705.1:c.3483A>T NP_001140177.1:p.Pro1161=
NM_001146706.1:c.3219A>T NP_001140178.1:p.Pro1073=
NM_004653.4:c.3390A>T NP_004644.2:p.Pro1130=
XM_005262560.1:c.3255A>T XP_005262617.1:p.Pro1085=
XM_005262561.1:c.3159A>T XP_005262618.1:p.Pro1053=
XM_011531468.1:c.3312A>T XP_011529770.1:p.Pro1104=
XR_244571.2:n.3678A>T
XR_430568.2:n.4012A>T
XM_005262560.3:c.3255A>T XP_005262617.1:p.Pro1085=
XM_005262561.3:c.3159A>T XP_005262618.1:p.Pro1053=
XM_011531468.3:c.3312A>T XP_011529770.1:p.Pro1104=
XM_024452495.1:c.1380A>T XP_024308263.1:p.Pro460=
XM_024452496.1:c.1146A>T XP_024308264.1:p.Pro382=
XR_001756009.2:n.4128A>T
XR_001756010.2:n.4128A>T
XR_001756011.2:n.3993A>T
XR_001756012.2:n.4141A>T
XR_001756013.2:n.3459A>T
XR_002958832.1:n.3560A>T
XR_002958834.1:n.3784A>T
XR_002958835.1:n.3667A>T
XR_002958836.1:n.4350A>T
XR_002958837.1:n.4157A>T
XR_244571.4:n.3677A>T
XR_430568.4:n.4011A>T
NM_001146706.2:c.3219A>T NP_001140178.1:p.Pro1073=
NM_004653.5:c.3390A>T MANE Select NP_004644.2:p.Pro1130=
NM_001146705.2:c.3483A>T NP_001140177.1:p.Pro1161=