Canonical Allele Identifier: CA2470565270

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918786C= , CM000686.2:g.12918786C=	GRCh38
NC_000024.9:g.15030698C= , CM000686.1:g.15030698C=	GRCh37
NC_000024.8:g.13540092C=	NCBI36
NG_012831.1:g.19680C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.*664C= MANE Select	ENSP00000336725.3:n.*664C=
ENST00000336079.7:c.*664C=	ENSP00000336725.3:n.*664C=
NM_004660.4:c.*664C=	NP_004651.2:n.*664C=
XM_006724878.1:c.*664C=	XP_006724941.1:n.*664C=
NM_001122665.3:c.*664C=	NP_001116137.1:n.*664C=
NM_001302552.2:c.*664C=	NP_001289481.1:n.*664C=
NM_001324195.1:c.*664C=	NP_001311124.1:n.*664C=
NR_136716.1:n.3116C=
NR_136717.1:n.2878C=
NR_136718.1:n.3196C=
NR_136719.1:n.2986C=
NR_136720.1:n.3047C=
NR_136721.1:n.2709C=
NR_136722.1:n.2793C=
NR_136723.1:n.3111C=
NR_136724.1:n.3031C=
XR_001756014.2:n.2811C=
NM_004660.5:c.*664C= MANE Select	NP_004651.2:n.*664C=
NM_001302552.3:c.*664C=	NP_001289481.1:n.*664C=
NM_001324195.2:c.*664C=	NP_001311124.1:n.*664C=
NR_136716.2:n.3034C=
NR_136717.2:n.2796C=
NR_136718.2:n.3114C=
NR_136719.2:n.2904C=
NR_136720.2:n.2965C=
NR_136721.2:n.2699C=