Canonical Allele Identifier: CA1139171465

Gene: DDX3Y

Linked Data

• gnomAD v3: Y-12918800-G-A
• gnomAD v4: Y-12918800-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918800G>A , CM000686.2:g.12918800G>A	GRCh38
NC_000024.9:g.15030712G>A , CM000686.1:g.15030712G>A	GRCh37
NC_000024.8:g.13540106G>A	NCBI36
NG_012831.1:g.19694G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.*678G>A MANE Select	ENSP00000336725.3:n.*678G>A
ENST00000336079.7:c.*678G>A	ENSP00000336725.3:n.*678G>A
NM_004660.4:c.*678G>A	NP_004651.2:n.*678G>A
XM_006724878.1:c.*678G>A	XP_006724941.1:n.*678G>A
NM_001122665.3:c.*678G>A	NP_001116137.1:n.*678G>A
NM_001302552.2:c.*678G>A	NP_001289481.1:n.*678G>A
NM_001324195.1:c.*678G>A	NP_001311124.1:n.*678G>A
NR_136716.1:n.3130G>A
NR_136717.1:n.2892G>A
NR_136718.1:n.3210G>A
NR_136719.1:n.3000G>A
NR_136720.1:n.3061G>A
NR_136721.1:n.2723G>A
NR_136722.1:n.2807G>A
NR_136723.1:n.3125G>A
NR_136724.1:n.3045G>A
XR_001756014.2:n.2825G>A
NM_004660.5:c.*678G>A MANE Select	NP_004651.2:n.*678G>A
NM_001302552.3:c.*678G>A	NP_001289481.1:n.*678G>A
NM_001324195.2:c.*678G>A	NP_001311124.1:n.*678G>A
NR_136716.2:n.3048G>A
NR_136717.2:n.2810G>A
NR_136718.2:n.3128G>A
NR_136719.2:n.2918G>A
NR_136720.2:n.2979G>A
NR_136721.2:n.2713G>A