Canonical Allele Identifier: CA2470565307

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12919473A= , CM000686.2:g.12919473A=	GRCh38
NC_000024.9:g.15031385A= , CM000686.1:g.15031385A=	GRCh37
NC_000024.8:g.13540779A=	NCBI36
NG_012831.1:g.20367A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004660.5:c.*1351A= MANE Select	NP_004651.2:n.*1351A=
ENST00000336079.8:c.*1351A= MANE Select	ENSP00000336725.3:n.*1351A=
NM_001122665.3:c.*1351A=	NP_001116137.1:n.*1351A=
NM_001302552.2:c.*1351A=	NP_001289481.1:n.*1351A=
NM_001302552.3:c.*1351A=	NP_001289481.1:n.*1351A=
NM_001324195.1:c.*1351A=	NP_001311124.1:n.*1351A=
NM_001324195.2:c.*1351A=	NP_001311124.1:n.*1351A=
NM_004660.4:c.*1351A=	NP_004651.2:n.*1351A=
NR_136716.1:n.3803A=
NR_136716.2:n.3721A=
NR_136717.1:n.3565A=
NR_136717.2:n.3483A=
NR_136718.1:n.3883A=
NR_136718.2:n.3801A=
NR_136719.1:n.3673A=
NR_136719.2:n.3591A=
NR_136720.1:n.3734A=
NR_136720.2:n.3652A=
NR_136721.1:n.3396A=
NR_136721.2:n.3386A=
NR_136722.1:n.3480A=
NR_136723.1:n.3798A=
NR_136724.1:n.3718A=
ENST00000336079.7:c.*1351A=	ENSP00000336725.3:n.*1351A=
XM_006724878.1:c.*1351A=	XP_006724941.1:n.*1351A=
XR_001756014.2:n.3498A=