Canonical Allele Identifier: CA414987754

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15027666A>C (hg19) ; chrY:g.12915754A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915754A>C , CM000686.2:g.12915754A>C	GRCh38
NC_000024.9:g.15027666A>C , CM000686.1:g.15027666A>C	GRCh37
NC_000024.8:g.13537060A>C	NCBI36
NG_012831.1:g.16648A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.1144A>C MANE Select	ENSP00000336725.3:p.Thr382Pro
ENST00000336079.7:c.1144A>C	ENSP00000336725.3:p.Thr382Pro
ENST00000360160.8:c.1144A>C	ENSP00000353284.4:p.Thr382Pro
ENST00000495478.1:n.259A>C
NM_001122665.2:c.1144A>C	NP_001116137.1:p.Thr382Pro
NM_001302552.1:c.1135A>C	NP_001289481.1:p.Thr379Pro
NM_004660.4:c.1144A>C	NP_004651.2:p.Thr382Pro
XM_006724878.1:c.1144A>C	XP_006724941.1:p.Thr382Pro
XM_011531471.1:c.1144A>C	XP_011529773.1:p.Thr382Pro
NM_001122665.3:c.1144A>C	NP_001116137.1:p.Thr382Pro
NM_001302552.2:c.1135A>C	NP_001289481.1:p.Thr379Pro
NM_001324195.1:c.1144A>C	NP_001311124.1:p.Thr382Pro
NR_136716.1:n.1613A>C
NR_136717.1:n.1375A>C
NR_136718.1:n.1693A>C
NR_136719.1:n.1483A>C
NR_136720.1:n.1613A>C
NR_136721.1:n.1206A>C
NR_136722.1:n.1290A>C
NR_136723.1:n.1608A>C
NR_136724.1:n.1528A>C
XR_001756014.2:n.1248A>C
NM_004660.5:c.1144A>C MANE Select	NP_004651.2:p.Thr382Pro
NM_001302552.3:c.1135A>C	NP_001289481.1:p.Thr379Pro
NM_001324195.2:c.1144A>C	NP_001311124.1:p.Thr382Pro
NR_136716.2:n.1531A>C
NR_136717.2:n.1293A>C
NR_136718.2:n.1611A>C
NR_136719.2:n.1401A>C
NR_136720.2:n.1531A>C
NR_136721.2:n.1196A>C