Canonical Allele Identifier: CA2579748425
Gene: DDX3Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12914515_12914516del , CM000686.2:g.12914515_12914516del GRCh38
NC_000024.9:g.15026427_15026428del , CM000686.1:g.15026427_15026428del GRCh37
NC_000024.8:g.13535821_13535822del NCBI36
NG_012831.1:g.15409_15410del

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.674-49_674-48del MANE Select ENSP00000336725.3:n.674-49_674-48del
ENST00000336079.7:c.674-49_674-48del ENSP00000336725.3:n.674-49_674-48del
ENST00000360160.8:c.674-49_674-48del ENSP00000353284.4:n.674-49_674-48del
ENST00000440554.1:c.665-49_665-48del ENSP00000400377.1:n.665-49_665-48del
ENST00000463199.1:n.192-49_192-48del
ENST00000472510.5:n.237-49_237-48del
NM_001122665.2:c.674-49_674-48del NP_001116137.1:n.674-49_674-48del
NM_001302552.1:c.665-49_665-48del NP_001289481.1:n.665-49_665-48del
NM_004660.4:c.674-49_674-48del NP_004651.2:n.674-49_674-48del
XM_006724878.1:c.674-49_674-48del XP_006724941.1:n.674-49_674-48del
XM_011531471.1:c.674-49_674-48del XP_011529773.1:n.674-49_674-48del
NM_001122665.3:c.674-49_674-48del NP_001116137.1:n.674-49_674-48del
NM_001302552.2:c.665-49_665-48del NP_001289481.1:n.665-49_665-48del
NM_001324195.1:c.674-49_674-48del NP_001311124.1:n.674-49_674-48del
NR_136716.1:n.825-49_825-48del
NR_136717.1:n.905-49_905-48del
NR_136718.1:n.905-49_905-48del
NR_136719.1:n.695-49_695-48del
NR_136720.1:n.825-49_825-48del
NR_136721.1:n.753-49_753-48del
NR_136722.1:n.820-49_820-48del
NR_136723.1:n.820-49_820-48del
NR_136724.1:n.740-49_740-48del
XR_001756014.2:n.778-49_778-48del
NM_004660.5:c.674-49_674-48del MANE Select NP_004651.2:n.674-49_674-48del
NM_001302552.3:c.665-49_665-48del NP_001289481.1:n.665-49_665-48del
NM_001324195.2:c.674-49_674-48del NP_001311124.1:n.674-49_674-48del
NR_136716.2:n.743-49_743-48del
NR_136717.2:n.823-49_823-48del
NR_136718.2:n.823-49_823-48del
NR_136719.2:n.613-49_613-48del
NR_136720.2:n.743-49_743-48del
NR_136721.2:n.743-49_743-48del