Canonical Allele Identifier: CA414840072
Gene: KDM5D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19706085G>T , CM000686.2:g.19706085G>T GRCh38
NC_000024.9:g.21867971G>T , CM000686.1:g.21867971G>T GRCh37
NC_000024.8:g.20327359G>T NCBI36
NG_032920.1:g.43855C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.4530C>A MANE Select ENSP00000322408.4:p.Ser1510Arg
ENST00000317961.8:c.4530C>A ENSP00000322408.4:p.Ser1510Arg
ENST00000382806.6:c.4359C>A ENSP00000372256.2:p.Ser1453Arg
ENST00000440077.5:c.4407C>A ENSP00000398543.1:p.Ser1469Arg
ENST00000469599.6:n.3281C>A
ENST00000492117.1:n.4575C>A
ENST00000541639.5:c.4623C>A ENSP00000444293.1:p.Ser1541Arg
NM_001146705.1:c.4623C>A NP_001140177.1:p.Ser1541Arg
NM_001146706.1:c.4359C>A NP_001140178.1:p.Ser1453Arg
NM_004653.4:c.4530C>A NP_004644.2:p.Ser1510Arg
XM_005262560.1:c.4395C>A XP_005262617.1:p.Ser1465Arg
XM_005262561.1:c.4299C>A XP_005262618.1:p.Ser1433Arg
XM_011531468.1:c.4452C>A XP_011529770.1:p.Ser1484Arg
XR_430568.2:n.5305C>A
XM_005262560.3:c.4395C>A XP_005262617.1:p.Ser1465Arg
XM_005262561.3:c.4299C>A XP_005262618.1:p.Ser1433Arg
XM_011531468.3:c.4452C>A XP_011529770.1:p.Ser1484Arg
XM_024452495.1:c.2520C>A XP_024308263.1:p.Ser840Arg
XM_024452496.1:c.2286C>A XP_024308264.1:p.Ser762Arg
XR_001756009.2:n.5268C>A
XR_001756010.2:n.5236C>A
XR_001756011.2:n.5133C>A
XR_001756012.2:n.5281C>A
XR_001756013.2:n.4599C>A
XR_002958832.1:n.4853C>A
XR_002958834.1:n.4924C>A
XR_002958835.1:n.4807C>A
XR_002958836.1:n.5458C>A
XR_002958837.1:n.5265C>A
XR_244571.4:n.4785C>A
XR_430568.4:n.5304C>A
NM_001146706.2:c.4359C>A NP_001140178.1:p.Ser1453Arg
NM_004653.5:c.4530C>A MANE Select NP_004644.2:p.Ser1510Arg
NM_001146705.2:c.4623C>A NP_001140177.1:p.Ser1541Arg