Canonical Allele Identifier: CA519898614

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15026558G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914646G>A , CM000686.2:g.12914646G>A	GRCh38
NC_000024.9:g.15026558G>A , CM000686.1:g.15026558G>A	GRCh37
NC_000024.8:g.13535952G>A	NCBI36
NG_012831.1:g.15540G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.756G>A MANE Select	ENSP00000336725.3:p.Val252=
ENST00000336079.7:c.756G>A	ENSP00000336725.3:p.Val252=
ENST00000360160.8:c.756G>A	ENSP00000353284.4:p.Val252=
ENST00000440554.1:c.747G>A	ENSP00000400377.1:p.Val249=
ENST00000463199.1:n.274G>A
ENST00000472510.5:n.319G>A
NM_001122665.2:c.756G>A	NP_001116137.1:p.Val252=
NM_001302552.1:c.747G>A	NP_001289481.1:p.Val249=
NM_004660.4:c.756G>A	NP_004651.2:p.Val252=
XM_006724878.1:c.756G>A	XP_006724941.1:p.Val252=
XM_011531471.1:c.756G>A	XP_011529773.1:p.Val252=
NM_001122665.3:c.756G>A	NP_001116137.1:p.Val252=
NM_001302552.2:c.747G>A	NP_001289481.1:p.Val249=
NM_001324195.1:c.756G>A	NP_001311124.1:p.Val252=
NR_136716.1:n.907G>A
NR_136717.1:n.987G>A
NR_136718.1:n.987G>A
NR_136719.1:n.777G>A
NR_136720.1:n.907G>A
NR_136721.1:n.835G>A
NR_136722.1:n.902G>A
NR_136723.1:n.902G>A
NR_136724.1:n.822G>A
XR_001756014.2:n.860G>A
NM_004660.5:c.756G>A MANE Select	NP_004651.2:p.Val252=
NM_001302552.3:c.747G>A	NP_001289481.1:p.Val249=
NM_001324195.2:c.756G>A	NP_001311124.1:p.Val252=
NR_136716.2:n.825G>A
NR_136717.2:n.905G>A
NR_136718.2:n.905G>A
NR_136719.2:n.695G>A
NR_136720.2:n.825G>A
NR_136721.2:n.825G>A