Canonical Allele Identifier: CA2556216916
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19705860G>A , CM000686.2:g.19705860G>A GRCh38
NC_000024.9:g.21867746G>A , CM000686.1:g.21867746G>A GRCh37
NC_000024.8:g.20327134G>A NCBI36
NG_032920.1:g.44080C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000317961.9:c.*135C>T MANE Select ENSP00000322408.4:n.*135C>T
ENST00000317961.8:c.*135C>T ENSP00000322408.4:n.*135C>T
ENST00000382806.6:c.*135C>T ENSP00000372256.2:n.*135C>T
ENST00000469599.6:n.3506C>T
ENST00000492117.1:n.4800C>T
ENST00000541639.5:c.*135C>T ENSP00000444293.1:n.*135C>T
NM_001146705.1:c.*135C>T NP_001140177.1:n.*135C>T
NM_001146706.1:c.*135C>T NP_001140178.1:n.*135C>T
NM_004653.4:c.*135C>T NP_004644.2:n.*135C>T
XM_005262560.1:c.*135C>T XP_005262617.1:n.*135C>T
XM_005262561.1:c.*135C>T XP_005262618.1:n.*135C>T
XM_011531468.1:c.*135C>T XP_011529770.1:n.*135C>T
XR_430568.2:n.5530C>T
XM_005262560.3:c.*135C>T XP_005262617.1:n.*135C>T
XM_005262561.3:c.*135C>T XP_005262618.1:n.*135C>T
XM_011531468.3:c.*135C>T XP_011529770.1:n.*135C>T
XM_024452495.1:c.*135C>T XP_024308263.1:n.*135C>T
XM_024452496.1:c.*135C>T XP_024308264.1:n.*135C>T
XR_001756009.2:n.5493C>T
XR_001756010.2:n.5461C>T
XR_001756011.2:n.5358C>T
XR_001756012.2:n.5506C>T
XR_001756013.2:n.4824C>T
XR_002958832.1:n.5078C>T
XR_002958834.1:n.5149C>T
XR_002958835.1:n.5032C>T
XR_002958836.1:n.5683C>T
XR_002958837.1:n.5490C>T
XR_244571.4:n.5010C>T
XR_430568.4:n.5529C>T
NM_001146706.2:c.*135C>T NP_001140178.1:n.*135C>T
NM_004653.5:c.*135C>T MANE Select NP_004644.2:n.*135C>T
NM_001146705.2:c.*135C>T NP_001140177.1:n.*135C>T