Canonical Allele Identifier: CA2470565262

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918732C= , CM000686.2:g.12918732C=	GRCh38
NC_000024.9:g.15030644C= , CM000686.1:g.15030644C=	GRCh37
NC_000024.8:g.13540038C=	NCBI36
NG_012831.1:g.19626C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.*610C= MANE Select	ENSP00000336725.3:n.*610C=
ENST00000336079.7:c.*610C=	ENSP00000336725.3:n.*610C=
NM_004660.4:c.*610C=	NP_004651.2:n.*610C=
XM_006724878.1:c.*610C=	XP_006724941.1:n.*610C=
NM_001122665.3:c.*610C=	NP_001116137.1:n.*610C=
NM_001302552.2:c.*610C=	NP_001289481.1:n.*610C=
NM_001324195.1:c.*610C=	NP_001311124.1:n.*610C=
NR_136716.1:n.3062C=
NR_136717.1:n.2824C=
NR_136718.1:n.3142C=
NR_136719.1:n.2932C=
NR_136720.1:n.2993C=
NR_136721.1:n.2655C=
NR_136722.1:n.2739C=
NR_136723.1:n.3057C=
NR_136724.1:n.2977C=
XR_001756014.2:n.2757C=
NM_004660.5:c.*610C= MANE Select	NP_004651.2:n.*610C=
NM_001302552.3:c.*610C=	NP_001289481.1:n.*610C=
NM_001324195.2:c.*610C=	NP_001311124.1:n.*610C=
NR_136716.2:n.2980C=
NR_136717.2:n.2742C=
NR_136718.2:n.3060C=
NR_136719.2:n.2850C=
NR_136720.2:n.2911C=
NR_136721.2:n.2645C=