Canonical Allele Identifier: CA2739260119

Gene: DDX3Y

Linked Data

• dbSNP Id: rs2148301155

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918615T>A , CM000686.2:g.12918615T>A	GRCh38
NC_000024.9:g.15030527T>A , CM000686.1:g.15030527T>A	GRCh37
NC_000024.8:g.13539921T>A	NCBI36
NG_012831.1:g.19509T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.*493T>A MANE Select	ENSP00000336725.3:n.*493T>A
ENST00000336079.7:c.*493T>A	ENSP00000336725.3:n.*493T>A
NM_004660.4:c.*493T>A	NP_004651.2:n.*493T>A
XM_006724878.1:c.*493T>A	XP_006724941.1:n.*493T>A
NM_001122665.3:c.*493T>A	NP_001116137.1:n.*493T>A
NM_001302552.2:c.*493T>A	NP_001289481.1:n.*493T>A
NM_001324195.1:c.*493T>A	NP_001311124.1:n.*493T>A
NR_136716.1:n.2945T>A
NR_136717.1:n.2707T>A
NR_136718.1:n.3025T>A
NR_136719.1:n.2815T>A
NR_136720.1:n.2876T>A
NR_136721.1:n.2538T>A
NR_136722.1:n.2622T>A
NR_136723.1:n.2940T>A
NR_136724.1:n.2860T>A
XR_001756014.2:n.2640T>A
NM_004660.5:c.*493T>A MANE Select	NP_004651.2:n.*493T>A
NM_001302552.3:c.*493T>A	NP_001289481.1:n.*493T>A
NM_001324195.2:c.*493T>A	NP_001311124.1:n.*493T>A
NR_136716.2:n.2863T>A
NR_136717.2:n.2625T>A
NR_136718.2:n.2943T>A
NR_136719.2:n.2733T>A
NR_136720.2:n.2794T>A
NR_136721.2:n.2528T>A