Canonical Allele Identifier: CA2766243451

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914847_12914857del , CM000686.2:g.12914847_12914857del	GRCh38
NC_000024.9:g.15026759_15026769del , CM000686.1:g.15026759_15026769del	GRCh37
NC_000024.8:g.13536153_13536163del	NCBI36
NG_012831.1:g.15741_15751del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336079.8:c.760-37_760-27del MANE Select	ENSP00000336725.3:n.760-37_760-27del
ENST00000336079.7:c.760-37_760-27del	ENSP00000336725.3:n.760-37_760-27del
ENST00000360160.8:c.760-37_760-27del	ENSP00000353284.4:n.760-37_760-27del
ENST00000463199.1:n.278-37_278-27del
ENST00000472510.5:n.520_530del
NM_001122665.2:c.760-37_760-27del	NP_001116137.1:n.760-37_760-27del
NM_001302552.1:c.751-37_751-27del	NP_001289481.1:n.751-37_751-27del
NM_004660.4:c.760-37_760-27del	NP_004651.2:n.760-37_760-27del
XM_006724878.1:c.760-37_760-27del	XP_006724941.1:n.760-37_760-27del
XM_011531471.1:c.760-37_760-27del	XP_011529773.1:n.760-37_760-27del
NM_001122665.3:c.760-37_760-27del	NP_001116137.1:n.760-37_760-27del
NM_001302552.2:c.751-37_751-27del	NP_001289481.1:n.751-37_751-27del
NM_001324195.1:c.760-37_760-27del	NP_001311124.1:n.760-37_760-27del
NR_136716.1:n.1108_1118del
NR_136717.1:n.991-37_991-27del
NR_136718.1:n.1188_1198del
NR_136719.1:n.978_988del
NR_136720.1:n.1108_1118del
NR_136721.1:n.839-37_839-27del
NR_136722.1:n.906-37_906-27del
NR_136723.1:n.1103_1113del
NR_136724.1:n.1023_1033del
XR_001756014.2:n.864-37_864-27del
NM_004660.5:c.760-37_760-27del MANE Select	NP_004651.2:n.760-37_760-27del
NM_001302552.3:c.751-37_751-27del	NP_001289481.1:n.751-37_751-27del
NM_001324195.2:c.760-37_760-27del	NP_001311124.1:n.760-37_760-27del
NR_136716.2:n.1026_1036del
NR_136717.2:n.909-37_909-27del
NR_136718.2:n.1106_1116del
NR_136719.2:n.896_906del
NR_136720.2:n.1026_1036del
NR_136721.2:n.829-37_829-27del