Canonical Allele Identifier: CA2470564467

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12907101C= , CM000686.2:g.12907101C=	GRCh38
NC_000024.9:g.15019012C= , CM000686.1:g.15019012C=	GRCh37
NC_000024.8:g.13528406C=	NCBI36
NG_012831.1:g.7994C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.46-436C= MANE Select	ENSP00000336725.3:n.46-436C=
ENST00000336079.7:c.46-436C=	ENSP00000336725.3:n.46-436C=
ENST00000360160.8:c.46-436C=	ENSP00000353284.4:n.46-436C=
ENST00000440554.1:c.37-436C=	ENSP00000400377.1:n.37-436C=
ENST00000454054.5:c.46-436C=	ENSP00000398953.1:n.46-436C=
ENST00000493363.1:n.134-436C=
NM_001122665.2:c.46-436C=	NP_001116137.1:n.46-436C=
NM_001302552.1:c.37-436C=	NP_001289481.1:n.37-436C=
NM_004660.4:c.46-436C=	NP_004651.2:n.46-436C=
XM_006724878.1:c.46-436C=	XP_006724941.1:n.46-436C=
XM_011531471.1:c.46-436C=	XP_011529773.1:n.46-436C=
NM_001122665.3:c.46-436C=	NP_001116137.1:n.46-436C=
NM_001302552.2:c.37-436C=	NP_001289481.1:n.37-436C=
NM_001324195.1:c.46-436C=	NP_001311124.1:n.46-436C=
NR_136716.1:n.197-436C=
NR_136717.1:n.197-436C=
NR_136718.1:n.197-436C=
NR_136719.1:n.197-436C=
NR_136720.1:n.197-436C=
NR_136721.1:n.125-436C=
NR_136722.1:n.112-436C=
NR_136723.1:n.112-436C=
NR_136724.1:n.112-436C=
XR_001756014.2:n.150-436C=
NM_004660.5:c.46-436C= MANE Select	NP_004651.2:n.46-436C=
NM_001302552.3:c.37-436C=	NP_001289481.1:n.37-436C=
NM_001324195.2:c.46-436C=	NP_001311124.1:n.46-436C=
NR_136716.2:n.115-436C=
NR_136717.2:n.115-436C=
NR_136718.2:n.115-436C=
NR_136719.2:n.115-436C=
NR_136720.2:n.115-436C=
NR_136721.2:n.115-436C=