Canonical Allele Identifier: CA414843284
Gene: KDM5D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707478C>G , CM000686.2:g.19707478C>G GRCh38
NC_000024.9:g.21869364C>G , CM000686.1:g.21869364C>G GRCh37
NC_000024.8:g.20328752C>G NCBI36
NG_032920.1:g.42462G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3668G>C MANE Select ENSP00000322408.4:p.Trp1223Ser
ENST00000317961.8:c.3668G>C ENSP00000322408.4:p.Trp1223Ser
ENST00000382806.6:c.3497G>C ENSP00000372256.2:p.Trp1166Ser
ENST00000415360.1:c.584G>C ENSP00000389433.1:p.Trp195Ser
ENST00000440077.5:c.3545G>C ENSP00000398543.1:p.Trp1182Ser
ENST00000469599.6:n.2266G>C
ENST00000492117.1:n.3560G>C
ENST00000541639.5:c.3761G>C ENSP00000444293.1:p.Trp1254Ser
NM_001146705.1:c.3761G>C NP_001140177.1:p.Trp1254Ser
NM_001146706.1:c.3497G>C NP_001140178.1:p.Trp1166Ser
NM_004653.4:c.3668G>C NP_004644.2:p.Trp1223Ser
XM_005262560.1:c.3533G>C XP_005262617.1:p.Trp1178Ser
XM_005262561.1:c.3437G>C XP_005262618.1:p.Trp1146Ser
XM_011531468.1:c.3590G>C XP_011529770.1:p.Trp1197Ser
XR_244571.2:n.3956G>C
XR_430568.2:n.4290G>C
XM_005262560.3:c.3533G>C XP_005262617.1:p.Trp1178Ser
XM_005262561.3:c.3437G>C XP_005262618.1:p.Trp1146Ser
XM_011531468.3:c.3590G>C XP_011529770.1:p.Trp1197Ser
XM_024452495.1:c.1658G>C XP_024308263.1:p.Trp553Ser
XM_024452496.1:c.1424G>C XP_024308264.1:p.Trp475Ser
XR_001756009.2:n.4406G>C
XR_001756010.2:n.4406G>C
XR_001756011.2:n.4271G>C
XR_001756012.2:n.4419G>C
XR_001756013.2:n.3737G>C
XR_002958832.1:n.3838G>C
XR_002958834.1:n.4062G>C
XR_002958835.1:n.3945G>C
XR_002958836.1:n.4628G>C
XR_002958837.1:n.4435G>C
XR_244571.4:n.3955G>C
XR_430568.4:n.4289G>C
NM_001146706.2:c.3497G>C NP_001140178.1:p.Trp1166Ser
NM_004653.5:c.3668G>C MANE Select NP_004644.2:p.Trp1223Ser
NM_001146705.2:c.3761G>C NP_001140177.1:p.Trp1254Ser