Canonical Allele Identifier: CA10573672

Gene: DDX3Y

Linked Data

• dbSNP Id: rs766386267
• ExAC: Y:15026602 A / G
• gnomAD v2: Y-15026602-A-G
• MyVariant Identifiers: chrY:g.15026602A>G (hg19) ; chrY:g.12914690A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914690A>G , CM000686.2:g.12914690A>G	GRCh38
NC_000024.9:g.15026602A>G , CM000686.1:g.15026602A>G	GRCh37
NC_000024.8:g.13535996A>G	NCBI36
NG_012831.1:g.15584A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.759+41A>G MANE Select	ENSP00000336725.3:n.759+41A>G
ENST00000336079.7:c.759+41A>G	ENSP00000336725.3:n.759+41A>G
ENST00000360160.8:c.759+41A>G	ENSP00000353284.4:n.759+41A>G
ENST00000463199.1:n.277+41A>G
ENST00000472510.5:n.363A>G
NM_001122665.2:c.759+41A>G	NP_001116137.1:n.759+41A>G
NM_001302552.1:c.750+41A>G	NP_001289481.1:n.750+41A>G
NM_004660.4:c.759+41A>G	NP_004651.2:n.759+41A>G
XM_006724878.1:c.759+41A>G	XP_006724941.1:n.759+41A>G
XM_011531471.1:c.759+41A>G	XP_011529773.1:n.759+41A>G
NM_001122665.3:c.759+41A>G	NP_001116137.1:n.759+41A>G
NM_001302552.2:c.750+41A>G	NP_001289481.1:n.750+41A>G
NM_001324195.1:c.759+41A>G	NP_001311124.1:n.759+41A>G
NR_136716.1:n.951A>G
NR_136717.1:n.990+41A>G
NR_136718.1:n.1031A>G
NR_136719.1:n.821A>G
NR_136720.1:n.951A>G
NR_136721.1:n.838+41A>G
NR_136722.1:n.905+41A>G
NR_136723.1:n.946A>G
NR_136724.1:n.866A>G
XR_001756014.2:n.863+41A>G
NM_004660.5:c.759+41A>G MANE Select	NP_004651.2:n.759+41A>G
NM_001302552.3:c.750+41A>G	NP_001289481.1:n.750+41A>G
NM_001324195.2:c.759+41A>G	NP_001311124.1:n.759+41A>G
NR_136716.2:n.869A>G
NR_136717.2:n.908+41A>G
NR_136718.2:n.949A>G
NR_136719.2:n.739A>G
NR_136720.2:n.869A>G
NR_136721.2:n.828+41A>G