Canonical Allele Identifier: CA520499309

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027800T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915888T>A , CM000686.2:g.12915888T>A	GRCh38
NC_000024.9:g.15027800T>A , CM000686.1:g.15027800T>A	GRCh37
NC_000024.8:g.13537194T>A	NCBI36
NG_012831.1:g.16782T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1170T>A MANE Select	ENSP00000336725.3:p.Leu390=
ENST00000336079.7:c.1170T>A	ENSP00000336725.3:p.Leu390=
ENST00000360160.8:c.1170T>A	ENSP00000353284.4:p.Leu390=
ENST00000495478.1:n.285T>A
NM_001122665.2:c.1170T>A	NP_001116137.1:p.Leu390=
NM_001302552.1:c.1161T>A	NP_001289481.1:p.Leu387=
NM_004660.4:c.1170T>A	NP_004651.2:p.Leu390=
XM_006724878.1:c.1170T>A	XP_006724941.1:p.Leu390=
XM_011531471.1:c.1170T>A	XP_011529773.1:p.Leu390=
NM_001122665.3:c.1170T>A	NP_001116137.1:p.Leu390=
NM_001302552.2:c.1161T>A	NP_001289481.1:p.Leu387=
NM_001324195.1:c.1170T>A	NP_001311124.1:p.Leu390=
NR_136716.1:n.1639T>A
NR_136717.1:n.1401T>A
NR_136718.1:n.1719T>A
NR_136719.1:n.1509T>A
NR_136720.1:n.1639T>A
NR_136721.1:n.1232T>A
NR_136722.1:n.1316T>A
NR_136723.1:n.1634T>A
NR_136724.1:n.1554T>A
XR_001756014.2:n.1274T>A
NM_004660.5:c.1170T>A MANE Select	NP_004651.2:p.Leu390=
NM_001302552.3:c.1161T>A	NP_001289481.1:p.Leu387=
NM_001324195.2:c.1170T>A	NP_001311124.1:p.Leu390=
NR_136716.2:n.1557T>A
NR_136717.2:n.1319T>A
NR_136718.2:n.1637T>A
NR_136719.2:n.1427T>A
NR_136720.2:n.1557T>A
NR_136721.2:n.1222T>A