Canonical Allele Identifier: CA2552200518
Gene: DDX3Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12917606del , CM000686.2:g.12917606del GRCh38
NC_000024.9:g.15029518del , CM000686.1:g.15029518del GRCh37
NC_000024.8:g.13538912del NCBI36
NG_012831.1:g.18500del

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.1903+64del MANE Select ENSP00000336725.3:n.1903+64del
ENST00000336079.7:c.1903+64del ENSP00000336725.3:n.1903+64del
ENST00000360160.8:c.1903+64del ENSP00000353284.4:n.1903+64del
NM_001122665.2:c.1903+64del NP_001116137.1:n.1903+64del
NM_001302552.1:c.1894+64del NP_001289481.1:n.1894+64del
NM_004660.4:c.1903+64del NP_004651.2:n.1903+64del
XM_006724878.1:c.1834+64del XP_006724941.1:n.1834+64del
NM_001122665.3:c.1903+64del NP_001116137.1:n.1903+64del
NM_001302552.2:c.1894+64del NP_001289481.1:n.1894+64del
NM_001324195.1:c.1834+64del NP_001311124.1:n.1834+64del
NR_136716.1:n.2372+64del
NR_136717.1:n.2134+64del
NR_136718.1:n.2452+64del
NR_136719.1:n.2242+64del
NR_136720.1:n.2303+64del
NR_136721.1:n.1965+64del
NR_136722.1:n.2049+64del
NR_136723.1:n.2367+64del
NR_136724.1:n.2287+64del
XR_001756014.2:n.2067+64del
NM_004660.5:c.1903+64del MANE Select NP_004651.2:n.1903+64del
NM_001302552.3:c.1894+64del NP_001289481.1:n.1894+64del
NM_001324195.2:c.1834+64del NP_001311124.1:n.1834+64del
NR_136716.2:n.2290+64del
NR_136717.2:n.2052+64del
NR_136718.2:n.2370+64del
NR_136719.2:n.2160+64del
NR_136720.2:n.2221+64del
NR_136721.2:n.1955+64del