Canonical Allele Identifier: CA2500476579
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19705740G>A , CM000686.2:g.19705740G>A GRCh38
NC_000024.9:g.21867626G>A , CM000686.1:g.21867626G>A GRCh37
NC_000024.8:g.20327014G>A NCBI36
NG_032920.1:g.44200C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000317961.9:c.*255C>T MANE Select ENSP00000322408.4:n.*255C>T
ENST00000317961.8:c.*255C>T ENSP00000322408.4:n.*255C>T
ENST00000382806.6:c.*255C>T ENSP00000372256.2:n.*255C>T
ENST00000469599.6:n.3626C>T
ENST00000492117.1:n.4920C>T
ENST00000541639.5:c.*255C>T ENSP00000444293.1:n.*255C>T
NM_001146705.1:c.*255C>T NP_001140177.1:n.*255C>T
NM_001146706.1:c.*255C>T NP_001140178.1:n.*255C>T
NM_004653.4:c.*255C>T NP_004644.2:n.*255C>T
XM_005262560.1:c.*255C>T XP_005262617.1:n.*255C>T
XM_005262561.1:c.*255C>T XP_005262618.1:n.*255C>T
XM_011531468.1:c.*255C>T XP_011529770.1:n.*255C>T
XR_430568.2:n.5650C>T
XM_005262560.3:c.*255C>T XP_005262617.1:n.*255C>T
XM_005262561.3:c.*255C>T XP_005262618.1:n.*255C>T
XM_011531468.3:c.*255C>T XP_011529770.1:n.*255C>T
XM_024452495.1:c.*255C>T XP_024308263.1:n.*255C>T
XM_024452496.1:c.*255C>T XP_024308264.1:n.*255C>T
XR_001756009.2:n.5613C>T
XR_001756010.2:n.5581C>T
XR_001756011.2:n.5478C>T
XR_001756012.2:n.5626C>T
XR_001756013.2:n.4944C>T
XR_002958832.1:n.5198C>T
XR_002958834.1:n.5269C>T
XR_002958835.1:n.5152C>T
XR_002958836.1:n.5803C>T
XR_002958837.1:n.5610C>T
XR_244571.4:n.5130C>T
XR_430568.4:n.5649C>T
NM_001146706.2:c.*255C>T NP_001140178.1:n.*255C>T
NM_004653.5:c.*255C>T MANE Select NP_004644.2:n.*255C>T
NM_001146705.2:c.*255C>T NP_001140177.1:n.*255C>T