Canonical Allele Identifier: CA2807046582
Gene: TOX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52542118_52542119insTA , CM000678.2:g.52542118_52542119insTA GRCh38
NC_000016.9:g.52576030_52576031insTA , CM000678.1:g.52576030_52576031insTA GRCh37
NC_000016.8:g.51133531_51133532insTA NCBI36
NG_012623.1:g.10684_10685insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000219746.14:c.87+4518_87+4519insTA MANE Select ENSP00000219746.9:n.87+4518_87+4519insTA
ENST00000219746.13:c.87+4518_87+4519insTA ENSP00000219746.9:n.87+4518_87+4519insTA
ENST00000407228.7:c.-100+5595_-100+5596insTA ENSP00000385705.3:n.-100+5595_-100+5596insTA
ENST00000563091.1:c.-22+5249_-22+5250insTA ENSP00000457401.1:n.-22+5249_-22+5250insTA
ENST00000568436.1:c.87+4518_87+4519insTA ENSP00000463843.1:n.87+4518_87+4519insTA
NM_001080430.2:c.87+4518_87+4519insTA NP_001073899.2:n.87+4518_87+4519insTA
NM_001146188.1:c.-100+5595_-100+5596insTA NP_001139660.1:n.-100+5595_-100+5596insTA
XM_005255892.2:c.87+4518_87+4519insTA XP_005255949.1:n.87+4518_87+4519insTA
XM_005255893.2:c.-100+4518_-100+4519insTA XP_005255950.1:n.-100+4518_-100+4519insTA
NM_001080430.3:c.87+4518_87+4519insTA NP_001073899.2:n.87+4518_87+4519insTA
NM_001146188.2:c.-100+5595_-100+5596insTA NP_001139660.1:n.-100+5595_-100+5596insTA
XM_005255892.3:c.87+4518_87+4519insTA XP_005255949.1:n.87+4518_87+4519insTA
NM_001080430.4:c.87+4518_87+4519insTA MANE Select NP_001073899.2:n.87+4518_87+4519insTA