Canonical Allele Identifier: CA2470565266

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918745T= , CM000686.2:g.12918745T=	GRCh38
NC_000024.9:g.15030657T= , CM000686.1:g.15030657T=	GRCh37
NC_000024.8:g.13540051T=	NCBI36
NG_012831.1:g.19639T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.*623T= MANE Select	ENSP00000336725.3:n.*623T=
ENST00000336079.7:c.*623T=	ENSP00000336725.3:n.*623T=
NM_004660.4:c.*623T=	NP_004651.2:n.*623T=
XM_006724878.1:c.*623T=	XP_006724941.1:n.*623T=
NM_001122665.3:c.*623T=	NP_001116137.1:n.*623T=
NM_001302552.2:c.*623T=	NP_001289481.1:n.*623T=
NM_001324195.1:c.*623T=	NP_001311124.1:n.*623T=
NR_136716.1:n.3075T=
NR_136717.1:n.2837T=
NR_136718.1:n.3155T=
NR_136719.1:n.2945T=
NR_136720.1:n.3006T=
NR_136721.1:n.2668T=
NR_136722.1:n.2752T=
NR_136723.1:n.3070T=
NR_136724.1:n.2990T=
XR_001756014.2:n.2770T=
NM_004660.5:c.*623T= MANE Select	NP_004651.2:n.*623T=
NM_001302552.3:c.*623T=	NP_001289481.1:n.*623T=
NM_001324195.2:c.*623T=	NP_001311124.1:n.*623T=
NR_136716.2:n.2993T=
NR_136717.2:n.2755T=
NR_136718.2:n.3073T=
NR_136719.2:n.2863T=
NR_136720.2:n.2924T=
NR_136721.2:n.2658T=