Canonical Allele Identifier: CA2766243448

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914814_12914819del , CM000686.2:g.12914814_12914819del	GRCh38
NC_000024.9:g.15026726_15026731del , CM000686.1:g.15026726_15026731del	GRCh37
NC_000024.8:g.13536120_13536125del	NCBI36
NG_012831.1:g.15708_15713del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.760-70_760-65del MANE Select	ENSP00000336725.3:n.760-70_760-65del
ENST00000336079.7:c.760-70_760-65del	ENSP00000336725.3:n.760-70_760-65del
ENST00000360160.8:c.760-70_760-65del	ENSP00000353284.4:n.760-70_760-65del
ENST00000463199.1:n.278-70_278-65del
ENST00000472510.5:n.487_492del
NM_001122665.2:c.760-70_760-65del	NP_001116137.1:n.760-70_760-65del
NM_001302552.1:c.751-70_751-65del	NP_001289481.1:n.751-70_751-65del
NM_004660.4:c.760-70_760-65del	NP_004651.2:n.760-70_760-65del
XM_006724878.1:c.760-70_760-65del	XP_006724941.1:n.760-70_760-65del
XM_011531471.1:c.760-70_760-65del	XP_011529773.1:n.760-70_760-65del
NM_001122665.3:c.760-70_760-65del	NP_001116137.1:n.760-70_760-65del
NM_001302552.2:c.751-70_751-65del	NP_001289481.1:n.751-70_751-65del
NM_001324195.1:c.760-70_760-65del	NP_001311124.1:n.760-70_760-65del
NR_136716.1:n.1075_1080del
NR_136717.1:n.991-70_991-65del
NR_136718.1:n.1155_1160del
NR_136719.1:n.945_950del
NR_136720.1:n.1075_1080del
NR_136721.1:n.839-70_839-65del
NR_136722.1:n.906-70_906-65del
NR_136723.1:n.1070_1075del
NR_136724.1:n.990_995del
XR_001756014.2:n.864-70_864-65del
NM_004660.5:c.760-70_760-65del MANE Select	NP_004651.2:n.760-70_760-65del
NM_001302552.3:c.751-70_751-65del	NP_001289481.1:n.751-70_751-65del
NM_001324195.2:c.760-70_760-65del	NP_001311124.1:n.760-70_760-65del
NR_136716.2:n.993_998del
NR_136717.2:n.909-70_909-65del
NR_136718.2:n.1073_1078del
NR_136719.2:n.863_868del
NR_136720.2:n.993_998del
NR_136721.2:n.829-70_829-65del