Canonical Allele Identifier: CA414987737

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027663G>A (hg19) ; chrY:g.12915751G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915751G>A , CM000686.2:g.12915751G>A	GRCh38
NC_000024.9:g.15027663G>A , CM000686.1:g.15027663G>A	GRCh37
NC_000024.8:g.13537057G>A	NCBI36
NG_012831.1:g.16645G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1141G>A MANE Select	ENSP00000336725.3:p.Ala381Thr
ENST00000336079.7:c.1141G>A	ENSP00000336725.3:p.Ala381Thr
ENST00000360160.8:c.1141G>A	ENSP00000353284.4:p.Ala381Thr
ENST00000495478.1:n.256G>A
NM_001122665.2:c.1141G>A	NP_001116137.1:p.Ala381Thr
NM_001302552.1:c.1132G>A	NP_001289481.1:p.Ala378Thr
NM_004660.4:c.1141G>A	NP_004651.2:p.Ala381Thr
XM_006724878.1:c.1141G>A	XP_006724941.1:p.Ala381Thr
XM_011531471.1:c.1141G>A	XP_011529773.1:p.Ala381Thr
NM_001122665.3:c.1141G>A	NP_001116137.1:p.Ala381Thr
NM_001302552.2:c.1132G>A	NP_001289481.1:p.Ala378Thr
NM_001324195.1:c.1141G>A	NP_001311124.1:p.Ala381Thr
NR_136716.1:n.1610G>A
NR_136717.1:n.1372G>A
NR_136718.1:n.1690G>A
NR_136719.1:n.1480G>A
NR_136720.1:n.1610G>A
NR_136721.1:n.1203G>A
NR_136722.1:n.1287G>A
NR_136723.1:n.1605G>A
NR_136724.1:n.1525G>A
XR_001756014.2:n.1245G>A
NM_004660.5:c.1141G>A MANE Select	NP_004651.2:p.Ala381Thr
NM_001302552.3:c.1132G>A	NP_001289481.1:p.Ala378Thr
NM_001324195.2:c.1141G>A	NP_001311124.1:p.Ala381Thr
NR_136716.2:n.1528G>A
NR_136717.2:n.1290G>A
NR_136718.2:n.1608G>A
NR_136719.2:n.1398G>A
NR_136720.2:n.1528G>A
NR_136721.2:n.1193G>A