Canonical Allele Identifier: CA2470565263

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918738C= , CM000686.2:g.12918738C=	GRCh38
NC_000024.9:g.15030650C= , CM000686.1:g.15030650C=	GRCh37
NC_000024.8:g.13540044C=	NCBI36
NG_012831.1:g.19632C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.*616C= MANE Select	ENSP00000336725.3:n.*616C=
ENST00000336079.7:c.*616C=	ENSP00000336725.3:n.*616C=
NM_004660.4:c.*616C=	NP_004651.2:n.*616C=
XM_006724878.1:c.*616C=	XP_006724941.1:n.*616C=
NM_001122665.3:c.*616C=	NP_001116137.1:n.*616C=
NM_001302552.2:c.*616C=	NP_001289481.1:n.*616C=
NM_001324195.1:c.*616C=	NP_001311124.1:n.*616C=
NR_136716.1:n.3068C=
NR_136717.1:n.2830C=
NR_136718.1:n.3148C=
NR_136719.1:n.2938C=
NR_136720.1:n.2999C=
NR_136721.1:n.2661C=
NR_136722.1:n.2745C=
NR_136723.1:n.3063C=
NR_136724.1:n.2983C=
XR_001756014.2:n.2763C=
NM_004660.5:c.*616C= MANE Select	NP_004651.2:n.*616C=
NM_001302552.3:c.*616C=	NP_001289481.1:n.*616C=
NM_001324195.2:c.*616C=	NP_001311124.1:n.*616C=
NR_136716.2:n.2986C=
NR_136717.2:n.2748C=
NR_136718.2:n.3066C=
NR_136719.2:n.2856C=
NR_136720.2:n.2917C=
NR_136721.2:n.2651C=