Canonical Allele Identifier: CA2470565282

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918966C= , CM000686.2:g.12918966C=	GRCh38
NC_000024.9:g.15030878C= , CM000686.1:g.15030878C=	GRCh37
NC_000024.8:g.13540272C=	NCBI36
NG_012831.1:g.19860C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004660.5:c.*844C= MANE Select	NP_004651.2:n.*844C=
ENST00000336079.8:c.*844C= MANE Select	ENSP00000336725.3:n.*844C=
NM_001122665.3:c.*844C=	NP_001116137.1:n.*844C=
NM_001302552.2:c.*844C=	NP_001289481.1:n.*844C=
NM_001302552.3:c.*844C=	NP_001289481.1:n.*844C=
NM_001324195.1:c.*844C=	NP_001311124.1:n.*844C=
NM_001324195.2:c.*844C=	NP_001311124.1:n.*844C=
NM_004660.4:c.*844C=	NP_004651.2:n.*844C=
NR_136716.1:n.3296C=
NR_136716.2:n.3214C=
NR_136717.1:n.3058C=
NR_136717.2:n.2976C=
NR_136718.1:n.3376C=
NR_136718.2:n.3294C=
NR_136719.1:n.3166C=
NR_136719.2:n.3084C=
NR_136720.1:n.3227C=
NR_136720.2:n.3145C=
NR_136721.1:n.2889C=
NR_136721.2:n.2879C=
NR_136722.1:n.2973C=
NR_136723.1:n.3291C=
NR_136724.1:n.3211C=
ENST00000336079.7:c.*844C=	ENSP00000336725.3:n.*844C=
XM_006724878.1:c.*844C=	XP_006724941.1:n.*844C=
XR_001756014.2:n.2991C=