Canonical Allele Identifier: CA2543911000
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19705915T>A , CM000686.2:g.19705915T>A GRCh38
NC_000024.9:g.21867801T>A , CM000686.1:g.21867801T>A GRCh37
NC_000024.8:g.20327189T>A NCBI36
NG_032920.1:g.44025A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000317961.9:c.*80A>T MANE Select ENSP00000322408.4:n.*80A>T
ENST00000317961.8:c.*80A>T ENSP00000322408.4:n.*80A>T
ENST00000382806.6:c.*80A>T ENSP00000372256.2:n.*80A>T
ENST00000469599.6:n.3451A>T
ENST00000492117.1:n.4745A>T
ENST00000541639.5:c.*80A>T ENSP00000444293.1:n.*80A>T
NM_001146705.1:c.*80A>T NP_001140177.1:n.*80A>T
NM_001146706.1:c.*80A>T NP_001140178.1:n.*80A>T
NM_004653.4:c.*80A>T NP_004644.2:n.*80A>T
XM_005262560.1:c.*80A>T XP_005262617.1:n.*80A>T
XM_005262561.1:c.*80A>T XP_005262618.1:n.*80A>T
XM_011531468.1:c.*80A>T XP_011529770.1:n.*80A>T
XR_430568.2:n.5475A>T
XM_005262560.3:c.*80A>T XP_005262617.1:n.*80A>T
XM_005262561.3:c.*80A>T XP_005262618.1:n.*80A>T
XM_011531468.3:c.*80A>T XP_011529770.1:n.*80A>T
XM_024452495.1:c.*80A>T XP_024308263.1:n.*80A>T
XM_024452496.1:c.*80A>T XP_024308264.1:n.*80A>T
XR_001756009.2:n.5438A>T
XR_001756010.2:n.5406A>T
XR_001756011.2:n.5303A>T
XR_001756012.2:n.5451A>T
XR_001756013.2:n.4769A>T
XR_002958832.1:n.5023A>T
XR_002958834.1:n.5094A>T
XR_002958835.1:n.4977A>T
XR_002958836.1:n.5628A>T
XR_002958837.1:n.5435A>T
XR_244571.4:n.4955A>T
XR_430568.4:n.5474A>T
NM_001146706.2:c.*80A>T NP_001140178.1:n.*80A>T
NM_004653.5:c.*80A>T MANE Select NP_004644.2:n.*80A>T
NM_001146705.2:c.*80A>T NP_001140177.1:n.*80A>T