Canonical Allele Identifier: CA2766243881

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12918812A>G , CM000686.2:g.12918812A>G	GRCh38
NC_000024.9:g.15030724A>G , CM000686.1:g.15030724A>G	GRCh37
NC_000024.8:g.13540118A>G	NCBI36
NG_012831.1:g.19706A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.*690A>G MANE Select	ENSP00000336725.3:n.*690A>G
ENST00000336079.7:c.*690A>G	ENSP00000336725.3:n.*690A>G
NM_004660.4:c.*690A>G	NP_004651.2:n.*690A>G
XM_006724878.1:c.*690A>G	XP_006724941.1:n.*690A>G
NM_001122665.3:c.*690A>G	NP_001116137.1:n.*690A>G
NM_001302552.2:c.*690A>G	NP_001289481.1:n.*690A>G
NM_001324195.1:c.*690A>G	NP_001311124.1:n.*690A>G
NR_136716.1:n.3142A>G
NR_136717.1:n.2904A>G
NR_136718.1:n.3222A>G
NR_136719.1:n.3012A>G
NR_136720.1:n.3073A>G
NR_136721.1:n.2735A>G
NR_136722.1:n.2819A>G
NR_136723.1:n.3137A>G
NR_136724.1:n.3057A>G
XR_001756014.2:n.2837A>G
NM_004660.5:c.*690A>G MANE Select	NP_004651.2:n.*690A>G
NM_001302552.3:c.*690A>G	NP_001289481.1:n.*690A>G
NM_001324195.2:c.*690A>G	NP_001311124.1:n.*690A>G
NR_136716.2:n.3060A>G
NR_136717.2:n.2822A>G
NR_136718.2:n.3140A>G
NR_136719.2:n.2930A>G
NR_136720.2:n.2991A>G
NR_136721.2:n.2725A>G