Canonical Allele Identifier: CA2470565039

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12915726C= , CM000686.2:g.12915726C=	GRCh38
NC_000024.9:g.15027638C= , CM000686.1:g.15027638C=	GRCh37
NC_000024.8:g.13537032C=	NCBI36
NG_012831.1:g.16620C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004660.5:c.1116C= MANE Select	NP_004651.2:p.Gly372=
ENST00000336079.8:c.1116C= MANE Select	ENSP00000336725.3:p.Gly372=
NM_001122665.2:c.1116C=	NP_001116137.1:p.Gly372=
NM_001122665.3:c.1116C=	NP_001116137.1:p.Gly372=
NM_001302552.1:c.1107C=	NP_001289481.1:p.Gly369=
NM_001302552.2:c.1107C=	NP_001289481.1:p.Gly369=
NM_001302552.3:c.1107C=	NP_001289481.1:p.Gly369=
NM_001324195.1:c.1116C=	NP_001311124.1:p.Gly372=
NM_001324195.2:c.1116C=	NP_001311124.1:p.Gly372=
NM_004660.4:c.1116C=	NP_004651.2:p.Gly372=
NR_136716.1:n.1585C=
NR_136716.2:n.1503C=
NR_136717.1:n.1347C=
NR_136717.2:n.1265C=
NR_136718.1:n.1665C=
NR_136718.2:n.1583C=
NR_136719.1:n.1455C=
NR_136719.2:n.1373C=
NR_136720.1:n.1585C=
NR_136720.2:n.1503C=
NR_136721.1:n.1178C=
NR_136721.2:n.1168C=
NR_136722.1:n.1262C=
NR_136723.1:n.1580C=
NR_136724.1:n.1500C=
ENST00000336079.7:c.1116C=	ENSP00000336725.3:p.Gly372=
ENST00000360160.8:c.1116C=	ENSP00000353284.4:p.Gly372=
ENST00000495478.1:n.231C=
XM_006724878.1:c.1116C=	XP_006724941.1:p.Gly372=
XM_011531471.1:c.1116C=	XP_011529773.1:p.Gly372=
XR_001756014.2:n.1220C=