Canonical Allele Identifier: CA2579748440
Gene: DDX3Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12914809T>C , CM000686.2:g.12914809T>C GRCh38
NC_000024.9:g.15026721T>C , CM000686.1:g.15026721T>C GRCh37
NC_000024.8:g.13536115T>C NCBI36
NG_012831.1:g.15703T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.760-75T>C MANE Select ENSP00000336725.3:n.760-75T>C
ENST00000336079.7:c.760-75T>C ENSP00000336725.3:n.760-75T>C
ENST00000360160.8:c.760-75T>C ENSP00000353284.4:n.760-75T>C
ENST00000463199.1:n.278-75T>C
ENST00000472510.5:n.482T>C
NM_001122665.2:c.760-75T>C NP_001116137.1:n.760-75T>C
NM_001302552.1:c.751-75T>C NP_001289481.1:n.751-75T>C
NM_004660.4:c.760-75T>C NP_004651.2:n.760-75T>C
XM_006724878.1:c.760-75T>C XP_006724941.1:n.760-75T>C
XM_011531471.1:c.760-75T>C XP_011529773.1:n.760-75T>C
NM_001122665.3:c.760-75T>C NP_001116137.1:n.760-75T>C
NM_001302552.2:c.751-75T>C NP_001289481.1:n.751-75T>C
NM_001324195.1:c.760-75T>C NP_001311124.1:n.760-75T>C
NR_136716.1:n.1070T>C
NR_136717.1:n.991-75T>C
NR_136718.1:n.1150T>C
NR_136719.1:n.940T>C
NR_136720.1:n.1070T>C
NR_136721.1:n.839-75T>C
NR_136722.1:n.906-75T>C
NR_136723.1:n.1065T>C
NR_136724.1:n.985T>C
XR_001756014.2:n.864-75T>C
NM_004660.5:c.760-75T>C MANE Select NP_004651.2:n.760-75T>C
NM_001302552.3:c.751-75T>C NP_001289481.1:n.751-75T>C
NM_001324195.2:c.760-75T>C NP_001311124.1:n.760-75T>C
NR_136716.2:n.988T>C
NR_136717.2:n.909-75T>C
NR_136718.2:n.1068T>C
NR_136719.2:n.858T>C
NR_136720.2:n.988T>C
NR_136721.2:n.829-75T>C