Canonical Allele Identifier: CA2470564958

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914696T= , CM000686.2:g.12914696T=	GRCh38
NC_000024.9:g.15026608T= , CM000686.1:g.15026608T=	GRCh37
NC_000024.8:g.13536002T=	NCBI36
NG_012831.1:g.15590T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.759+47T= MANE Select	ENSP00000336725.3:n.759+47T=
ENST00000336079.7:c.759+47T=	ENSP00000336725.3:n.759+47T=
ENST00000360160.8:c.759+47T=	ENSP00000353284.4:n.759+47T=
ENST00000463199.1:n.277+47T=
ENST00000472510.5:n.369T=
NM_001122665.2:c.759+47T=	NP_001116137.1:n.759+47T=
NM_001302552.1:c.750+47T=	NP_001289481.1:n.750+47T=
NM_004660.4:c.759+47T=	NP_004651.2:n.759+47T=
XM_006724878.1:c.759+47T=	XP_006724941.1:n.759+47T=
XM_011531471.1:c.759+47T=	XP_011529773.1:n.759+47T=
NM_001122665.3:c.759+47T=	NP_001116137.1:n.759+47T=
NM_001302552.2:c.750+47T=	NP_001289481.1:n.750+47T=
NM_001324195.1:c.759+47T=	NP_001311124.1:n.759+47T=
NR_136716.1:n.957T=
NR_136717.1:n.990+47T=
NR_136718.1:n.1037T=
NR_136719.1:n.827T=
NR_136720.1:n.957T=
NR_136721.1:n.838+47T=
NR_136722.1:n.905+47T=
NR_136723.1:n.952T=
NR_136724.1:n.872T=
XR_001756014.2:n.863+47T=
NM_004660.5:c.759+47T= MANE Select	NP_004651.2:n.759+47T=
NM_001302552.3:c.750+47T=	NP_001289481.1:n.750+47T=
NM_001324195.2:c.759+47T=	NP_001311124.1:n.759+47T=
NR_136716.2:n.875T=
NR_136717.2:n.908+47T=
NR_136718.2:n.955T=
NR_136719.2:n.745T=
NR_136720.2:n.875T=
NR_136721.2:n.828+47T=