Canonical Allele Identifier: CA2470564948

Gene: DDX3Y

Genomic Alleles

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

Transcript Alleles

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