Canonical Allele Identifier: CA2766243407

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12914511_12914516del , CM000686.2:g.12914511_12914516del	GRCh38

Transcript Alleles

HGVS	Amino-acid change
ENST00000336079.8:c.674-53_674-48del MANE Select	ENSP00000336725.3:n.674-53_674-48del
ENST00000336079.7:c.674-53_674-48del	ENSP00000336725.3:n.674-53_674-48del
ENST00000360160.8:c.674-53_674-48del	ENSP00000353284.4:n.674-53_674-48del
ENST00000440554.1:c.665-53_665-48del	ENSP00000400377.1:n.665-53_665-48del
ENST00000463199.1:n.192-53_192-48del
ENST00000472510.5:n.237-53_237-48del
NM_001122665.2:c.674-53_674-48del	NP_001116137.1:n.674-53_674-48del
NM_001302552.1:c.665-53_665-48del	NP_001289481.1:n.665-53_665-48del
NM_004660.4:c.674-53_674-48del	NP_004651.2:n.674-53_674-48del
XM_006724878.1:c.674-53_674-48del	XP_006724941.1:n.674-53_674-48del
XM_011531471.1:c.674-53_674-48del	XP_011529773.1:n.674-53_674-48del
NM_001122665.3:c.674-53_674-48del	NP_001116137.1:n.674-53_674-48del
NM_001302552.2:c.665-53_665-48del	NP_001289481.1:n.665-53_665-48del
NM_001324195.1:c.674-53_674-48del	NP_001311124.1:n.674-53_674-48del
NR_136716.1:n.825-53_825-48del
NR_136717.1:n.905-53_905-48del
NR_136718.1:n.905-53_905-48del
NR_136719.1:n.695-53_695-48del
NR_136720.1:n.825-53_825-48del
NR_136721.1:n.753-53_753-48del
NR_136722.1:n.820-53_820-48del
NR_136723.1:n.820-53_820-48del
NR_136724.1:n.740-53_740-48del
XR_001756014.2:n.778-53_778-48del
NM_004660.5:c.674-53_674-48del MANE Select	NP_004651.2:n.674-53_674-48del
NM_001302552.3:c.665-53_665-48del	NP_001289481.1:n.665-53_665-48del
NM_001324195.2:c.674-53_674-48del	NP_001311124.1:n.674-53_674-48del
NR_136716.2:n.743-53_743-48del
NR_136717.2:n.823-53_823-48del
NR_136718.2:n.823-53_823-48del
NR_136719.2:n.613-53_613-48del
NR_136720.2:n.743-53_743-48del
NR_136721.2:n.743-53_743-48del