Canonical Allele Identifier: CA337722329

Gene: DDX3Y

Linked Data

• dbSNP Id: rs773551747
• gnomAD v3: Y-12918786-C-G
• gnomAD v4: Y-12918786-C-G
• MyVariant Identifiers: chrY:g.15030698C>G (hg19) ; chrY:g.12918786C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918786C>G , CM000686.2:g.12918786C>G	GRCh38
NC_000024.9:g.15030698C>G , CM000686.1:g.15030698C>G	GRCh37
NC_000024.8:g.13540092C>G	NCBI36
NG_012831.1:g.19680C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.*664C>G MANE Select	ENSP00000336725.3:n.*664C>G
ENST00000336079.7:c.*664C>G	ENSP00000336725.3:n.*664C>G
NM_004660.4:c.*664C>G	NP_004651.2:n.*664C>G
XM_006724878.1:c.*664C>G	XP_006724941.1:n.*664C>G
NM_001122665.3:c.*664C>G	NP_001116137.1:n.*664C>G
NM_001302552.2:c.*664C>G	NP_001289481.1:n.*664C>G
NM_001324195.1:c.*664C>G	NP_001311124.1:n.*664C>G
NR_136716.1:n.3116C>G
NR_136717.1:n.2878C>G
NR_136718.1:n.3196C>G
NR_136719.1:n.2986C>G
NR_136720.1:n.3047C>G
NR_136721.1:n.2709C>G
NR_136722.1:n.2793C>G
NR_136723.1:n.3111C>G
NR_136724.1:n.3031C>G
XR_001756014.2:n.2811C>G
NM_004660.5:c.*664C>G MANE Select	NP_004651.2:n.*664C>G
NM_001302552.3:c.*664C>G	NP_001289481.1:n.*664C>G
NM_001324195.2:c.*664C>G	NP_001311124.1:n.*664C>G
NR_136716.2:n.3034C>G
NR_136717.2:n.2796C>G
NR_136718.2:n.3114C>G
NR_136719.2:n.2904C>G
NR_136720.2:n.2965C>G
NR_136721.2:n.2699C>G