Canonical Allele Identifier: CA2766243525
Gene: DDX3Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12915492_12915494del , CM000686.2:g.12915492_12915494del GRCh38
NC_000024.9:g.15027404_15027406del , CM000686.1:g.15027404_15027406del GRCh37
NC_000024.8:g.13536798_13536800del NCBI36
NG_012831.1:g.16386_16388del

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.1020-138_1020-136del MANE Select ENSP00000336725.3:n.1020-138_1020-136del
ENST00000336079.7:c.1020-138_1020-136del ENSP00000336725.3:n.1020-138_1020-136del
ENST00000360160.8:c.1020-138_1020-136del ENSP00000353284.4:n.1020-138_1020-136del
NM_001122665.2:c.1020-138_1020-136del NP_001116137.1:n.1020-138_1020-136del
NM_001302552.1:c.1011-138_1011-136del NP_001289481.1:n.1011-138_1011-136del
NM_004660.4:c.1020-138_1020-136del NP_004651.2:n.1020-138_1020-136del
XM_006724878.1:c.1020-138_1020-136del XP_006724941.1:n.1020-138_1020-136del
XM_011531471.1:c.1020-138_1020-136del XP_011529773.1:n.1020-138_1020-136del
NM_001122665.3:c.1020-138_1020-136del NP_001116137.1:n.1020-138_1020-136del
NM_001302552.2:c.1011-138_1011-136del NP_001289481.1:n.1011-138_1011-136del
NM_001324195.1:c.1020-138_1020-136del NP_001311124.1:n.1020-138_1020-136del
NR_136716.1:n.1489-138_1489-136del
NR_136717.1:n.1251-138_1251-136del
NR_136718.1:n.1569-138_1569-136del
NR_136719.1:n.1359-138_1359-136del
NR_136720.1:n.1489-138_1489-136del
NR_136721.1:n.1082-138_1082-136del
NR_136722.1:n.1166-138_1166-136del
NR_136723.1:n.1484-138_1484-136del
NR_136724.1:n.1404-138_1404-136del
XR_001756014.2:n.1124-138_1124-136del
NM_004660.5:c.1020-138_1020-136del MANE Select NP_004651.2:n.1020-138_1020-136del
NM_001302552.3:c.1011-138_1011-136del NP_001289481.1:n.1011-138_1011-136del
NM_001324195.2:c.1020-138_1020-136del NP_001311124.1:n.1020-138_1020-136del
NR_136716.2:n.1407-138_1407-136del
NR_136717.2:n.1169-138_1169-136del
NR_136718.2:n.1487-138_1487-136del
NR_136719.2:n.1277-138_1277-136del
NR_136720.2:n.1407-138_1407-136del
NR_136721.2:n.1072-138_1072-136del