Canonical Allele Identifier: CA2470564949

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914632G= , CM000686.2:g.12914632G=	GRCh38
NC_000024.9:g.15026544G= , CM000686.1:g.15026544G=	GRCh37
NC_000024.8:g.13535938G=	NCBI36
NG_012831.1:g.15526G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.742G= MANE Select	ENSP00000336725.3:p.Ala248=
ENST00000336079.7:c.742G=	ENSP00000336725.3:p.Ala248=
ENST00000360160.8:c.742G=	ENSP00000353284.4:p.Ala248=
ENST00000440554.1:c.733G=	ENSP00000400377.1:p.Ala245=
ENST00000463199.1:n.260G=
ENST00000472510.5:n.305G=
NM_001122665.2:c.742G=	NP_001116137.1:p.Ala248=
NM_001302552.1:c.733G=	NP_001289481.1:p.Ala245=
NM_004660.4:c.742G=	NP_004651.2:p.Ala248=
XM_006724878.1:c.742G=	XP_006724941.1:p.Ala248=
XM_011531471.1:c.742G=	XP_011529773.1:p.Ala248=
NM_001122665.3:c.742G=	NP_001116137.1:p.Ala248=
NM_001302552.2:c.733G=	NP_001289481.1:p.Ala245=
NM_001324195.1:c.742G=	NP_001311124.1:p.Ala248=
NR_136716.1:n.893G=
NR_136717.1:n.973G=
NR_136718.1:n.973G=
NR_136719.1:n.763G=
NR_136720.1:n.893G=
NR_136721.1:n.821G=
NR_136722.1:n.888G=
NR_136723.1:n.888G=
NR_136724.1:n.808G=
XR_001756014.2:n.846G=
NM_004660.5:c.742G= MANE Select	NP_004651.2:p.Ala248=
NM_001302552.3:c.733G=	NP_001289481.1:p.Ala245=
NM_001324195.2:c.742G=	NP_001311124.1:p.Ala248=
NR_136716.2:n.811G=
NR_136717.2:n.891G=
NR_136718.2:n.891G=
NR_136719.2:n.681G=
NR_136720.2:n.811G=
NR_136721.2:n.811G=