Canonical Allele Identifier: CA2566573411
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19727037G>A , CM000686.2:g.19727037G>A GRCh38
NC_000024.9:g.21888923G>A , CM000686.1:g.21888923G>A GRCh37
NC_000024.8:g.20348311G>A NCBI36
NG_032920.1:g.22903C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000317961.9:c.1371+4735C>T MANE Select ENSP00000322408.4:n.1371+4735C>T
ENST00000317961.8:c.1371+4735C>T ENSP00000322408.4:n.1371+4735C>T
ENST00000382806.6:c.1200+4735C>T ENSP00000372256.2:n.1200+4735C>T
ENST00000440077.5:c.1248+4735C>T ENSP00000398543.1:n.1248+4735C>T
ENST00000447300.1:c.1236+4735C>T ENSP00000416377.1:n.1236+4735C>T
ENST00000541639.5:c.1372-3604C>T ENSP00000444293.1:n.1372-3604C>T
NM_001146705.1:c.1372-3604C>T NP_001140177.1:n.1372-3604C>T
NM_001146706.1:c.1200+4735C>T NP_001140178.1:n.1200+4735C>T
NM_004653.4:c.1371+4735C>T NP_004644.2:n.1371+4735C>T
XM_005262560.1:c.1236+4735C>T XP_005262617.1:n.1236+4735C>T
XM_005262561.1:c.1371+4735C>T XP_005262618.1:n.1371+4735C>T
XM_005262562.2:c.1371+4735C>T XP_005262619.1:n.1371+4735C>T
XM_011531468.1:c.1371+4735C>T XP_011529770.1:n.1371+4735C>T
XR_244571.2:n.1659+4735C>T
XR_430568.2:n.1659+4735C>T
XR_938609.1:n.1659+4735C>T
XR_938610.1:n.1659+4735C>T
XM_005262560.3:c.1236+4735C>T XP_005262617.1:n.1236+4735C>T
XM_005262561.3:c.1371+4735C>T XP_005262618.1:n.1371+4735C>T
XM_011531468.3:c.1371+4735C>T XP_011529770.1:n.1371+4735C>T
XM_024452495.1:c.-747+4735C>T XP_024308263.1:n.-747+4735C>T
XR_001756009.2:n.1658+4735C>T
XR_001756010.2:n.1658+4735C>T
XR_001756011.2:n.1523+4735C>T
XR_001756012.2:n.1658+4735C>T
XR_001756013.2:n.1658+4735C>T
XR_002958832.1:n.1658+4735C>T
XR_002958833.1:n.1658+4735C>T
XR_002958834.1:n.1658+4735C>T
XR_002958835.1:n.1658+4735C>T
XR_002958836.1:n.1658+4735C>T
XR_002958837.1:n.1658+4735C>T
XR_244571.4:n.1658+4735C>T
XR_430568.4:n.1658+4735C>T
NM_001146706.2:c.1200+4735C>T NP_001140178.1:n.1200+4735C>T
NM_004653.5:c.1371+4735C>T MANE Select NP_004644.2:n.1371+4735C>T
NM_001146705.2:c.1372-3604C>T NP_001140177.1:n.1372-3604C>T