Canonical Allele Identifier: CA2766243444
Gene: DDX3Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12914786T>A , CM000686.2:g.12914786T>A GRCh38
NC_000024.9:g.15026698T>A , CM000686.1:g.15026698T>A GRCh37
NC_000024.8:g.13536092T>A NCBI36
NG_012831.1:g.15680T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000336079.8:c.760-98T>A MANE Select ENSP00000336725.3:n.760-98T>A
ENST00000336079.7:c.760-98T>A ENSP00000336725.3:n.760-98T>A
ENST00000360160.8:c.760-98T>A ENSP00000353284.4:n.760-98T>A
ENST00000463199.1:n.278-98T>A
ENST00000472510.5:n.459T>A
NM_001122665.2:c.760-98T>A NP_001116137.1:n.760-98T>A
NM_001302552.1:c.751-98T>A NP_001289481.1:n.751-98T>A
NM_004660.4:c.760-98T>A NP_004651.2:n.760-98T>A
XM_006724878.1:c.760-98T>A XP_006724941.1:n.760-98T>A
XM_011531471.1:c.760-98T>A XP_011529773.1:n.760-98T>A
NM_001122665.3:c.760-98T>A NP_001116137.1:n.760-98T>A
NM_001302552.2:c.751-98T>A NP_001289481.1:n.751-98T>A
NM_001324195.1:c.760-98T>A NP_001311124.1:n.760-98T>A
NR_136716.1:n.1047T>A
NR_136717.1:n.991-98T>A
NR_136718.1:n.1127T>A
NR_136719.1:n.917T>A
NR_136720.1:n.1047T>A
NR_136721.1:n.839-98T>A
NR_136722.1:n.906-98T>A
NR_136723.1:n.1042T>A
NR_136724.1:n.962T>A
XR_001756014.2:n.864-98T>A
NM_004660.5:c.760-98T>A MANE Select NP_004651.2:n.760-98T>A
NM_001302552.3:c.751-98T>A NP_001289481.1:n.751-98T>A
NM_001324195.2:c.760-98T>A NP_001311124.1:n.760-98T>A
NR_136716.2:n.965T>A
NR_136717.2:n.909-98T>A
NR_136718.2:n.1045T>A
NR_136719.2:n.835T>A
NR_136720.2:n.965T>A
NR_136721.2:n.829-98T>A