Canonical Allele Identifier: CA2470565269

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918780G= , CM000686.2:g.12918780G=	GRCh38
NC_000024.9:g.15030692G= , CM000686.1:g.15030692G=	GRCh37
NC_000024.8:g.13540086G=	NCBI36
NG_012831.1:g.19674G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.*658G= MANE Select	ENSP00000336725.3:n.*658G=
ENST00000336079.7:c.*658G=	ENSP00000336725.3:n.*658G=
NM_004660.4:c.*658G=	NP_004651.2:n.*658G=
XM_006724878.1:c.*658G=	XP_006724941.1:n.*658G=
NM_001122665.3:c.*658G=	NP_001116137.1:n.*658G=
NM_001302552.2:c.*658G=	NP_001289481.1:n.*658G=
NM_001324195.1:c.*658G=	NP_001311124.1:n.*658G=
NR_136716.1:n.3110G=
NR_136717.1:n.2872G=
NR_136718.1:n.3190G=
NR_136719.1:n.2980G=
NR_136720.1:n.3041G=
NR_136721.1:n.2703G=
NR_136722.1:n.2787G=
NR_136723.1:n.3105G=
NR_136724.1:n.3025G=
XR_001756014.2:n.2805G=
NM_004660.5:c.*658G= MANE Select	NP_004651.2:n.*658G=
NM_001302552.3:c.*658G=	NP_001289481.1:n.*658G=
NM_001324195.2:c.*658G=	NP_001311124.1:n.*658G=
NR_136716.2:n.3028G=
NR_136717.2:n.2790G=
NR_136718.2:n.3108G=
NR_136719.2:n.2898G=
NR_136720.2:n.2959G=
NR_136721.2:n.2693G=