Canonical Allele Identifier: CA2470565267

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918752T= , CM000686.2:g.12918752T=	GRCh38
NC_000024.9:g.15030664T= , CM000686.1:g.15030664T=	GRCh37
NC_000024.8:g.13540058T=	NCBI36
NG_012831.1:g.19646T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.*630T= MANE Select	ENSP00000336725.3:n.*630T=
ENST00000336079.7:c.*630T=	ENSP00000336725.3:n.*630T=
NM_004660.4:c.*630T=	NP_004651.2:n.*630T=
XM_006724878.1:c.*630T=	XP_006724941.1:n.*630T=
NM_001122665.3:c.*630T=	NP_001116137.1:n.*630T=
NM_001302552.2:c.*630T=	NP_001289481.1:n.*630T=
NM_001324195.1:c.*630T=	NP_001311124.1:n.*630T=
NR_136716.1:n.3082T=
NR_136717.1:n.2844T=
NR_136718.1:n.3162T=
NR_136719.1:n.2952T=
NR_136720.1:n.3013T=
NR_136721.1:n.2675T=
NR_136722.1:n.2759T=
NR_136723.1:n.3077T=
NR_136724.1:n.2997T=
XR_001756014.2:n.2777T=
NM_004660.5:c.*630T= MANE Select	NP_004651.2:n.*630T=
NM_001302552.3:c.*630T=	NP_001289481.1:n.*630T=
NM_001324195.2:c.*630T=	NP_001311124.1:n.*630T=
NR_136716.2:n.3000T=
NR_136717.2:n.2762T=
NR_136718.2:n.3080T=
NR_136719.2:n.2870T=
NR_136720.2:n.2931T=
NR_136721.2:n.2665T=