Canonical Allele Identifier: CA2222759778
Gene: TOX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52514304_52514305delinsGC , CM000678.2:g.52514304_52514305delinsGC GRCh38
NC_000016.9:g.52548216_52548217delinsGC , CM000678.1:g.52548216_52548217delinsGC GRCh37
NC_000016.8:g.51105717_51105718delinsGC NCBI36
NG_012623.1:g.38498_38499delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000219746.14:c.87+32332_87+32333delinsGC MANE Select ENSP00000219746.9:n.87+32332_87+32333delinsGC
ENST00000219746.13:c.87+32332_87+32333delinsGC ENSP00000219746.9:n.87+32332_87+32333delinsGC
ENST00000407228.7:c.75+5101_75+5102delinsGC ENSP00000385705.3:n.75+5101_75+5102delinsGC
ENST00000563091.1:c.-22+33063_-22+33064delinsGC ENSP00000457401.1:n.-22+33063_-22+33064delinsGC
ENST00000568436.1:c.87+32332_87+32333delinsGC ENSP00000463843.1:n.87+32332_87+32333delinsGC
NM_001080430.2:c.87+32332_87+32333delinsGC NP_001073899.2:n.87+32332_87+32333delinsGC
NM_001146188.1:c.75+5101_75+5102delinsGC NP_001139660.1:n.75+5101_75+5102delinsGC
XM_005255892.2:c.87+32332_87+32333delinsGC XP_005255949.1:n.87+32332_87+32333delinsGC
XM_005255893.2:c.75+5101_75+5102delinsGC XP_005255950.1:n.75+5101_75+5102delinsGC
NM_001080430.3:c.87+32332_87+32333delinsGC NP_001073899.2:n.87+32332_87+32333delinsGC
NM_001146188.2:c.75+5101_75+5102delinsGC NP_001139660.1:n.75+5101_75+5102delinsGC
XM_005255892.3:c.87+32332_87+32333delinsGC XP_005255949.1:n.87+32332_87+32333delinsGC
XM_017023142.1:c.75+5101_75+5102delinsGC XP_016878631.1:n.75+5101_75+5102delinsGC
XM_024450230.1:c.75+5101_75+5102delinsGC XP_024305998.1:n.75+5101_75+5102delinsGC
NM_001080430.4:c.87+32332_87+32333delinsGC MANE Select NP_001073899.2:n.87+32332_87+32333delinsGC