Canonical Allele Identifier: CA2571503470
Gene: DDX3Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12914836del , CM000686.2:g.12914836del GRCh38
NC_000024.9:g.15026748del , CM000686.1:g.15026748del GRCh37
NC_000024.8:g.13536142del NCBI36
NG_012831.1:g.15730del

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.760-48del MANE Select ENSP00000336725.3:n.760-48del
ENST00000336079.7:c.760-48del ENSP00000336725.3:n.760-48del
ENST00000360160.8:c.760-48del ENSP00000353284.4:n.760-48del
ENST00000463199.1:n.278-48del
ENST00000472510.5:n.509del
NM_001122665.2:c.760-48del NP_001116137.1:n.760-48del
NM_001302552.1:c.751-48del NP_001289481.1:n.751-48del
NM_004660.4:c.760-48del NP_004651.2:n.760-48del
XM_006724878.1:c.760-48del XP_006724941.1:n.760-48del
XM_011531471.1:c.760-48del XP_011529773.1:n.760-48del
NM_001122665.3:c.760-48del NP_001116137.1:n.760-48del
NM_001302552.2:c.751-48del NP_001289481.1:n.751-48del
NM_001324195.1:c.760-48del NP_001311124.1:n.760-48del
NR_136716.1:n.1097del
NR_136717.1:n.991-48del
NR_136718.1:n.1177del
NR_136719.1:n.967del
NR_136720.1:n.1097del
NR_136721.1:n.839-48del
NR_136722.1:n.906-48del
NR_136723.1:n.1092del
NR_136724.1:n.1012del
XR_001756014.2:n.864-48del
NM_004660.5:c.760-48del MANE Select NP_004651.2:n.760-48del
NM_001302552.3:c.751-48del NP_001289481.1:n.751-48del
NM_001324195.2:c.760-48del NP_001311124.1:n.760-48del
NR_136716.2:n.1015del
NR_136717.2:n.909-48del
NR_136718.2:n.1095del
NR_136719.2:n.885del
NR_136720.2:n.1015del
NR_136721.2:n.829-48del