Canonical Allele Identifier: CA2470565277

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918855T= , CM000686.2:g.12918855T=	GRCh38
NC_000024.9:g.15030767T= , CM000686.1:g.15030767T=	GRCh37
NC_000024.8:g.13540161T=	NCBI36
NG_012831.1:g.19749T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.*733T= MANE Select	ENSP00000336725.3:n.*733T=
ENST00000336079.7:c.*733T=	ENSP00000336725.3:n.*733T=
NM_004660.4:c.*733T=	NP_004651.2:n.*733T=
XM_006724878.1:c.*733T=	XP_006724941.1:n.*733T=
NM_001122665.3:c.*733T=	NP_001116137.1:n.*733T=
NM_001302552.2:c.*733T=	NP_001289481.1:n.*733T=
NM_001324195.1:c.*733T=	NP_001311124.1:n.*733T=
NR_136716.1:n.3185T=
NR_136717.1:n.2947T=
NR_136718.1:n.3265T=
NR_136719.1:n.3055T=
NR_136720.1:n.3116T=
NR_136721.1:n.2778T=
NR_136722.1:n.2862T=
NR_136723.1:n.3180T=
NR_136724.1:n.3100T=
XR_001756014.2:n.2880T=
NM_004660.5:c.*733T= MANE Select	NP_004651.2:n.*733T=
NM_001302552.3:c.*733T=	NP_001289481.1:n.*733T=
NM_001324195.2:c.*733T=	NP_001311124.1:n.*733T=
NR_136716.2:n.3103T=
NR_136717.2:n.2865T=
NR_136718.2:n.3183T=
NR_136719.2:n.2973T=
NR_136720.2:n.3034T=
NR_136721.2:n.2768T=