Canonical Allele Identifier: CA1139171411

Gene: DDX3Y

Linked Data

• dbSNP Id: rs2053658152
• gnomAD v3: Y-12918675-C-T
• gnomAD v4: Y-12918675-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918675C>T , CM000686.2:g.12918675C>T	GRCh38
NC_000024.9:g.15030587C>T , CM000686.1:g.15030587C>T	GRCh37
NC_000024.8:g.13539981C>T	NCBI36
NG_012831.1:g.19569C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.*553C>T MANE Select	ENSP00000336725.3:n.*553C>T
ENST00000336079.7:c.*553C>T	ENSP00000336725.3:n.*553C>T
NM_004660.4:c.*553C>T	NP_004651.2:n.*553C>T
XM_006724878.1:c.*553C>T	XP_006724941.1:n.*553C>T
NM_001122665.3:c.*553C>T	NP_001116137.1:n.*553C>T
NM_001302552.2:c.*553C>T	NP_001289481.1:n.*553C>T
NM_001324195.1:c.*553C>T	NP_001311124.1:n.*553C>T
NR_136716.1:n.3005C>T
NR_136717.1:n.2767C>T
NR_136718.1:n.3085C>T
NR_136719.1:n.2875C>T
NR_136720.1:n.2936C>T
NR_136721.1:n.2598C>T
NR_136722.1:n.2682C>T
NR_136723.1:n.3000C>T
NR_136724.1:n.2920C>T
XR_001756014.2:n.2700C>T
NM_004660.5:c.*553C>T MANE Select	NP_004651.2:n.*553C>T
NM_001302552.3:c.*553C>T	NP_001289481.1:n.*553C>T
NM_001324195.2:c.*553C>T	NP_001311124.1:n.*553C>T
NR_136716.2:n.2923C>T
NR_136717.2:n.2685C>T
NR_136718.2:n.3003C>T
NR_136719.2:n.2793C>T
NR_136720.2:n.2854C>T
NR_136721.2:n.2588C>T