Canonical Allele Identifier: CA414842088
Gene: KDM5D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19732708C>A , CM000686.2:g.19732708C>A GRCh38
NC_000024.9:g.21894594C>A , CM000686.1:g.21894594C>A GRCh37
NC_000024.8:g.20353982C>A NCBI36
NG_032920.1:g.17232G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.968G>T MANE Select ENSP00000322408.4:p.Gly323Val
ENST00000317961.8:c.968G>T ENSP00000322408.4:p.Gly323Val
ENST00000382806.6:c.797G>T ENSP00000372256.2:p.Gly266Val
ENST00000440077.5:c.845G>T ENSP00000398543.1:p.Gly282Val
ENST00000447300.1:c.833G>T ENSP00000416377.1:p.Gly278Val
ENST00000541639.5:c.968G>T ENSP00000444293.1:p.Gly323Val
NM_001146705.1:c.968G>T NP_001140177.1:p.Gly323Val
NM_001146706.1:c.797G>T NP_001140178.1:p.Gly266Val
NM_004653.4:c.968G>T NP_004644.2:p.Gly323Val
XM_005262560.1:c.833G>T XP_005262617.1:p.Gly278Val
XM_005262561.1:c.968G>T XP_005262618.1:p.Gly323Val
XM_005262562.2:c.968G>T XP_005262619.1:p.Gly323Val
XM_011531468.1:c.968G>T XP_011529770.1:p.Gly323Val
XR_244571.2:n.1256G>T
XR_430568.2:n.1256G>T
XR_938609.1:n.1256G>T
XR_938610.1:n.1256G>T
XM_005262560.3:c.833G>T XP_005262617.1:p.Gly278Val
XM_005262561.3:c.968G>T XP_005262618.1:p.Gly323Val
XM_011531468.3:c.968G>T XP_011529770.1:p.Gly323Val
XM_024452495.1:c.-1150G>T XP_024308263.1:n.-1150G>T
XR_001756009.2:n.1255G>T
XR_001756010.2:n.1255G>T
XR_001756011.2:n.1120G>T
XR_001756012.2:n.1255G>T
XR_001756013.2:n.1255G>T
XR_002958832.1:n.1255G>T
XR_002958833.1:n.1255G>T
XR_002958834.1:n.1255G>T
XR_002958835.1:n.1255G>T
XR_002958836.1:n.1255G>T
XR_002958837.1:n.1255G>T
XR_244571.4:n.1255G>T
XR_430568.4:n.1255G>T
NM_001146706.2:c.797G>T NP_001140178.1:p.Gly266Val
NM_004653.5:c.968G>T MANE Select NP_004644.2:p.Gly323Val
NM_001146705.2:c.968G>T NP_001140177.1:p.Gly323Val