Canonical Allele Identifier: CA2579748524
Gene: DDX3Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12917595_12917599del , CM000686.2:g.12917595_12917599del GRCh38
NC_000024.9:g.15029507_15029511del , CM000686.1:g.15029507_15029511del GRCh37
NC_000024.8:g.13538901_13538905del NCBI36
NG_012831.1:g.18489_18493del

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.1903+53_1903+57del MANE Select ENSP00000336725.3:n.1903+53_1903+57del
ENST00000336079.7:c.1903+53_1903+57del ENSP00000336725.3:n.1903+53_1903+57del
ENST00000360160.8:c.1903+53_1903+57del ENSP00000353284.4:n.1903+53_1903+57del
NM_001122665.2:c.1903+53_1903+57del NP_001116137.1:n.1903+53_1903+57del
NM_001302552.1:c.1894+53_1894+57del NP_001289481.1:n.1894+53_1894+57del
NM_004660.4:c.1903+53_1903+57del NP_004651.2:n.1903+53_1903+57del
XM_006724878.1:c.1834+53_1834+57del XP_006724941.1:n.1834+53_1834+57del
NM_001122665.3:c.1903+53_1903+57del NP_001116137.1:n.1903+53_1903+57del
NM_001302552.2:c.1894+53_1894+57del NP_001289481.1:n.1894+53_1894+57del
NM_001324195.1:c.1834+53_1834+57del NP_001311124.1:n.1834+53_1834+57del
NR_136716.1:n.2372+53_2372+57del
NR_136717.1:n.2134+53_2134+57del
NR_136718.1:n.2452+53_2452+57del
NR_136719.1:n.2242+53_2242+57del
NR_136720.1:n.2303+53_2303+57del
NR_136721.1:n.1965+53_1965+57del
NR_136722.1:n.2049+53_2049+57del
NR_136723.1:n.2367+53_2367+57del
NR_136724.1:n.2287+53_2287+57del
XR_001756014.2:n.2067+53_2067+57del
NM_004660.5:c.1903+53_1903+57del MANE Select NP_004651.2:n.1903+53_1903+57del
NM_001302552.3:c.1894+53_1894+57del NP_001289481.1:n.1894+53_1894+57del
NM_001324195.2:c.1834+53_1834+57del NP_001311124.1:n.1834+53_1834+57del
NR_136716.2:n.2290+53_2290+57del
NR_136717.2:n.2052+53_2052+57del
NR_136718.2:n.2370+53_2370+57del
NR_136719.2:n.2160+53_2160+57del
NR_136720.2:n.2221+53_2221+57del
NR_136721.2:n.1955+53_1955+57del