Canonical Allele Identifier: CA10573671

Gene: DDX3Y

Linked Data

• dbSNP Id: rs760764178
• ExAC: Y:15026578 A / C
• gnomAD v2: Y-15026578-A-C
• gnomAD v3: Y-12914666-A-C
• gnomAD v4: Y-12914666-A-C
• MyVariant Identifiers: chrY:g.15026578A>C (hg19) ; chrY:g.12914666A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914666A>C , CM000686.2:g.12914666A>C	GRCh38
NC_000024.9:g.15026578A>C , CM000686.1:g.15026578A>C	GRCh37
NC_000024.8:g.13535972A>C	NCBI36
NG_012831.1:g.15560A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.759+17A>C MANE Select	ENSP00000336725.3:n.759+17A>C
ENST00000336079.7:c.759+17A>C	ENSP00000336725.3:n.759+17A>C
ENST00000360160.8:c.759+17A>C	ENSP00000353284.4:n.759+17A>C
ENST00000463199.1:n.277+17A>C
ENST00000472510.5:n.339A>C
NM_001122665.2:c.759+17A>C	NP_001116137.1:n.759+17A>C
NM_001302552.1:c.750+17A>C	NP_001289481.1:n.750+17A>C
NM_004660.4:c.759+17A>C	NP_004651.2:n.759+17A>C
XM_006724878.1:c.759+17A>C	XP_006724941.1:n.759+17A>C
XM_011531471.1:c.759+17A>C	XP_011529773.1:n.759+17A>C
NM_001122665.3:c.759+17A>C	NP_001116137.1:n.759+17A>C
NM_001302552.2:c.750+17A>C	NP_001289481.1:n.750+17A>C
NM_001324195.1:c.759+17A>C	NP_001311124.1:n.759+17A>C
NR_136716.1:n.927A>C
NR_136717.1:n.990+17A>C
NR_136718.1:n.1007A>C
NR_136719.1:n.797A>C
NR_136720.1:n.927A>C
NR_136721.1:n.838+17A>C
NR_136722.1:n.905+17A>C
NR_136723.1:n.922A>C
NR_136724.1:n.842A>C
XR_001756014.2:n.863+17A>C
NM_004660.5:c.759+17A>C MANE Select	NP_004651.2:n.759+17A>C
NM_001302552.3:c.750+17A>C	NP_001289481.1:n.750+17A>C
NM_001324195.2:c.759+17A>C	NP_001311124.1:n.759+17A>C
NR_136716.2:n.845A>C
NR_136717.2:n.908+17A>C
NR_136718.2:n.925A>C
NR_136719.2:n.715A>C
NR_136720.2:n.845A>C
NR_136721.2:n.828+17A>C