Canonical Allele Identifier: CA2545228366

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918755G>A , CM000686.2:g.12918755G>A	GRCh38
NC_000024.9:g.15030667G>A , CM000686.1:g.15030667G>A	GRCh37
NC_000024.8:g.13540061G>A	NCBI36
NG_012831.1:g.19649G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.*633G>A MANE Select	ENSP00000336725.3:n.*633G>A
ENST00000336079.7:c.*633G>A	ENSP00000336725.3:n.*633G>A
NM_004660.4:c.*633G>A	NP_004651.2:n.*633G>A
XM_006724878.1:c.*633G>A	XP_006724941.1:n.*633G>A
NM_001122665.3:c.*633G>A	NP_001116137.1:n.*633G>A
NM_001302552.2:c.*633G>A	NP_001289481.1:n.*633G>A
NM_001324195.1:c.*633G>A	NP_001311124.1:n.*633G>A
NR_136716.1:n.3085G>A
NR_136717.1:n.2847G>A
NR_136718.1:n.3165G>A
NR_136719.1:n.2955G>A
NR_136720.1:n.3016G>A
NR_136721.1:n.2678G>A
NR_136722.1:n.2762G>A
NR_136723.1:n.3080G>A
NR_136724.1:n.3000G>A
XR_001756014.2:n.2780G>A
NM_004660.5:c.*633G>A MANE Select	NP_004651.2:n.*633G>A
NM_001302552.3:c.*633G>A	NP_001289481.1:n.*633G>A
NM_001324195.2:c.*633G>A	NP_001311124.1:n.*633G>A
NR_136716.2:n.3003G>A
NR_136717.2:n.2765G>A
NR_136718.2:n.3083G>A
NR_136719.2:n.2873G>A
NR_136720.2:n.2934G>A
NR_136721.2:n.2668G>A