Canonical Allele Identifier: CA2470565271

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918794G= , CM000686.2:g.12918794G=	GRCh38
NC_000024.9:g.15030706G= , CM000686.1:g.15030706G=	GRCh37
NC_000024.8:g.13540100G=	NCBI36
NG_012831.1:g.19688G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.*672G= MANE Select	ENSP00000336725.3:n.*672G=
ENST00000336079.7:c.*672G=	ENSP00000336725.3:n.*672G=
NM_004660.4:c.*672G=	NP_004651.2:n.*672G=
XM_006724878.1:c.*672G=	XP_006724941.1:n.*672G=
NM_001122665.3:c.*672G=	NP_001116137.1:n.*672G=
NM_001302552.2:c.*672G=	NP_001289481.1:n.*672G=
NM_001324195.1:c.*672G=	NP_001311124.1:n.*672G=
NR_136716.1:n.3124G=
NR_136717.1:n.2886G=
NR_136718.1:n.3204G=
NR_136719.1:n.2994G=
NR_136720.1:n.3055G=
NR_136721.1:n.2717G=
NR_136722.1:n.2801G=
NR_136723.1:n.3119G=
NR_136724.1:n.3039G=
XR_001756014.2:n.2819G=
NM_004660.5:c.*672G= MANE Select	NP_004651.2:n.*672G=
NM_001302552.3:c.*672G=	NP_001289481.1:n.*672G=
NM_001324195.2:c.*672G=	NP_001311124.1:n.*672G=
NR_136716.2:n.3042G=
NR_136717.2:n.2804G=
NR_136718.2:n.3122G=
NR_136719.2:n.2912G=
NR_136720.2:n.2973G=
NR_136721.2:n.2707G=