Canonical Allele Identifier: CA2766253134
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19705907A>T , CM000686.2:g.19705907A>T GRCh38
NC_000024.9:g.21867793A>T , CM000686.1:g.21867793A>T GRCh37
NC_000024.8:g.20327181A>T NCBI36
NG_032920.1:g.44033T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.*88T>A MANE Select ENSP00000322408.4:n.*88T>A
ENST00000317961.8:c.*88T>A ENSP00000322408.4:n.*88T>A
ENST00000382806.6:c.*88T>A ENSP00000372256.2:n.*88T>A
ENST00000469599.6:n.3459T>A
ENST00000492117.1:n.4753T>A
ENST00000541639.5:c.*88T>A ENSP00000444293.1:n.*88T>A
NM_001146705.1:c.*88T>A NP_001140177.1:n.*88T>A
NM_001146706.1:c.*88T>A NP_001140178.1:n.*88T>A
NM_004653.4:c.*88T>A NP_004644.2:n.*88T>A
XM_005262560.1:c.*88T>A XP_005262617.1:n.*88T>A
XM_005262561.1:c.*88T>A XP_005262618.1:n.*88T>A
XM_011531468.1:c.*88T>A XP_011529770.1:n.*88T>A
XR_430568.2:n.5483T>A
XM_005262560.3:c.*88T>A XP_005262617.1:n.*88T>A
XM_005262561.3:c.*88T>A XP_005262618.1:n.*88T>A
XM_011531468.3:c.*88T>A XP_011529770.1:n.*88T>A
XM_024452495.1:c.*88T>A XP_024308263.1:n.*88T>A
XM_024452496.1:c.*88T>A XP_024308264.1:n.*88T>A
XR_001756009.2:n.5446T>A
XR_001756010.2:n.5414T>A
XR_001756011.2:n.5311T>A
XR_001756012.2:n.5459T>A
XR_001756013.2:n.4777T>A
XR_002958832.1:n.5031T>A
XR_002958834.1:n.5102T>A
XR_002958835.1:n.4985T>A
XR_002958836.1:n.5636T>A
XR_002958837.1:n.5443T>A
XR_244571.4:n.4963T>A
XR_430568.4:n.5482T>A
NM_001146706.2:c.*88T>A NP_001140178.1:n.*88T>A
NM_004653.5:c.*88T>A MANE Select NP_004644.2:n.*88T>A
NM_001146705.2:c.*88T>A NP_001140177.1:n.*88T>A