Canonical Allele Identifier: CA2470565310

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12919504G= , CM000686.2:g.12919504G=	GRCh38
NC_000024.9:g.15031416G= , CM000686.1:g.15031416G=	GRCh37
NC_000024.8:g.13540810G=	NCBI36
NG_012831.1:g.20398G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004660.5:c.*1382G= MANE Select	NP_004651.2:n.*1382G=
ENST00000336079.8:c.*1382G= MANE Select	ENSP00000336725.3:n.*1382G=
NM_001122665.3:c.*1382G=	NP_001116137.1:n.*1382G=
NM_001302552.2:c.*1382G=	NP_001289481.1:n.*1382G=
NM_001302552.3:c.*1382G=	NP_001289481.1:n.*1382G=
NM_001324195.1:c.*1382G=	NP_001311124.1:n.*1382G=
NM_001324195.2:c.*1382G=	NP_001311124.1:n.*1382G=
NM_004660.4:c.*1382G=	NP_004651.2:n.*1382G=
NR_136716.1:n.3834G=
NR_136716.2:n.3752G=
NR_136717.1:n.3596G=
NR_136717.2:n.3514G=
NR_136718.1:n.3914G=
NR_136718.2:n.3832G=
NR_136719.1:n.3704G=
NR_136719.2:n.3622G=
NR_136720.1:n.3765G=
NR_136720.2:n.3683G=
NR_136721.1:n.3427G=
NR_136721.2:n.3417G=
NR_136722.1:n.3511G=
NR_136723.1:n.3829G=
NR_136724.1:n.3749G=
ENST00000336079.7:c.*1382G=	ENSP00000336725.3:n.*1382G=
XM_006724878.1:c.*1382G=	XP_006724941.1:n.*1382G=
XR_001756014.2:n.3529G=