Canonical Allele Identifier: CA519898483

Gene: DDX3Y

Linked Data

• MyVariant Identifiers: chrY:g.15026543A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914631A>G , CM000686.2:g.12914631A>G	GRCh38
NC_000024.9:g.15026543A>G , CM000686.1:g.15026543A>G	GRCh37
NC_000024.8:g.13535937A>G	NCBI36
NG_012831.1:g.15525A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.741A>G MANE Select	ENSP00000336725.3:p.Glu247=
ENST00000336079.7:c.741A>G	ENSP00000336725.3:p.Glu247=
ENST00000360160.8:c.741A>G	ENSP00000353284.4:p.Glu247=
ENST00000440554.1:c.732A>G	ENSP00000400377.1:p.Glu244=
ENST00000463199.1:n.259A>G
ENST00000472510.5:n.304A>G
NM_001122665.2:c.741A>G	NP_001116137.1:p.Glu247=
NM_001302552.1:c.732A>G	NP_001289481.1:p.Glu244=
NM_004660.4:c.741A>G	NP_004651.2:p.Glu247=
XM_006724878.1:c.741A>G	XP_006724941.1:p.Glu247=
XM_011531471.1:c.741A>G	XP_011529773.1:p.Glu247=
NM_001122665.3:c.741A>G	NP_001116137.1:p.Glu247=
NM_001302552.2:c.732A>G	NP_001289481.1:p.Glu244=
NM_001324195.1:c.741A>G	NP_001311124.1:p.Glu247=
NR_136716.1:n.892A>G
NR_136717.1:n.972A>G
NR_136718.1:n.972A>G
NR_136719.1:n.762A>G
NR_136720.1:n.892A>G
NR_136721.1:n.820A>G
NR_136722.1:n.887A>G
NR_136723.1:n.887A>G
NR_136724.1:n.807A>G
XR_001756014.2:n.845A>G
NM_004660.5:c.741A>G MANE Select	NP_004651.2:p.Glu247=
NM_001302552.3:c.732A>G	NP_001289481.1:p.Glu244=
NM_001324195.2:c.741A>G	NP_001311124.1:p.Glu247=
NR_136716.2:n.810A>G
NR_136717.2:n.890A>G
NR_136718.2:n.890A>G
NR_136719.2:n.680A>G
NR_136720.2:n.810A>G
NR_136721.2:n.810A>G