Canonical Allele Identifier: CA414987149

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027561G>A (hg19) ; chrY:g.12915649G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915649G>A , CM000686.2:g.12915649G>A	GRCh38
NC_000024.9:g.15027561G>A , CM000686.1:g.15027561G>A	GRCh37
NC_000024.8:g.13536955G>A	NCBI36
NG_012831.1:g.16543G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1039G>A MANE Select	ENSP00000336725.3:p.Ala347Thr
ENST00000336079.7:c.1039G>A	ENSP00000336725.3:p.Ala347Thr
ENST00000360160.8:c.1039G>A	ENSP00000353284.4:p.Ala347Thr
ENST00000495478.1:n.154G>A
NM_001122665.2:c.1039G>A	NP_001116137.1:p.Ala347Thr
NM_001302552.1:c.1030G>A	NP_001289481.1:p.Ala344Thr
NM_004660.4:c.1039G>A	NP_004651.2:p.Ala347Thr
XM_006724878.1:c.1039G>A	XP_006724941.1:p.Ala347Thr
XM_011531471.1:c.1039G>A	XP_011529773.1:p.Ala347Thr
NM_001122665.3:c.1039G>A	NP_001116137.1:p.Ala347Thr
NM_001302552.2:c.1030G>A	NP_001289481.1:p.Ala344Thr
NM_001324195.1:c.1039G>A	NP_001311124.1:p.Ala347Thr
NR_136716.1:n.1508G>A
NR_136717.1:n.1270G>A
NR_136718.1:n.1588G>A
NR_136719.1:n.1378G>A
NR_136720.1:n.1508G>A
NR_136721.1:n.1101G>A
NR_136722.1:n.1185G>A
NR_136723.1:n.1503G>A
NR_136724.1:n.1423G>A
XR_001756014.2:n.1143G>A
NM_004660.5:c.1039G>A MANE Select	NP_004651.2:p.Ala347Thr
NM_001302552.3:c.1030G>A	NP_001289481.1:p.Ala344Thr
NM_001324195.2:c.1039G>A	NP_001311124.1:p.Ala347Thr
NR_136716.2:n.1426G>A
NR_136717.2:n.1188G>A
NR_136718.2:n.1506G>A
NR_136719.2:n.1296G>A
NR_136720.2:n.1426G>A
NR_136721.2:n.1091G>A