Canonical Allele Identifier: CA2470564973

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914833A= , CM000686.2:g.12914833A=	GRCh38
NC_000024.9:g.15026745A= , CM000686.1:g.15026745A=	GRCh37
NC_000024.8:g.13536139A=	NCBI36
NG_012831.1:g.15727A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.760-51A= MANE Select	ENSP00000336725.3:n.760-51A=
ENST00000336079.7:c.760-51A=	ENSP00000336725.3:n.760-51A=
ENST00000360160.8:c.760-51A=	ENSP00000353284.4:n.760-51A=
ENST00000463199.1:n.278-51A=
ENST00000472510.5:n.506A=
NM_001122665.2:c.760-51A=	NP_001116137.1:n.760-51A=
NM_001302552.1:c.751-51A=	NP_001289481.1:n.751-51A=
NM_004660.4:c.760-51A=	NP_004651.2:n.760-51A=
XM_006724878.1:c.760-51A=	XP_006724941.1:n.760-51A=
XM_011531471.1:c.760-51A=	XP_011529773.1:n.760-51A=
NM_001122665.3:c.760-51A=	NP_001116137.1:n.760-51A=
NM_001302552.2:c.751-51A=	NP_001289481.1:n.751-51A=
NM_001324195.1:c.760-51A=	NP_001311124.1:n.760-51A=
NR_136716.1:n.1094A=
NR_136717.1:n.991-51A=
NR_136718.1:n.1174A=
NR_136719.1:n.964A=
NR_136720.1:n.1094A=
NR_136721.1:n.839-51A=
NR_136722.1:n.906-51A=
NR_136723.1:n.1089A=
NR_136724.1:n.1009A=
XR_001756014.2:n.864-51A=
NM_004660.5:c.760-51A= MANE Select	NP_004651.2:n.760-51A=
NM_001302552.3:c.751-51A=	NP_001289481.1:n.751-51A=
NM_001324195.2:c.760-51A=	NP_001311124.1:n.760-51A=
NR_136716.2:n.1012A=
NR_136717.2:n.909-51A=
NR_136718.2:n.1092A=
NR_136719.2:n.882A=
NR_136720.2:n.1012A=
NR_136721.2:n.829-51A=