Canonical Allele Identifier: CA2222759949
Gene: TOX3 HGNC NCBI

Linked Data

dbSNP Id: rs1962390314

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52514461_52514462insG , CM000678.2:g.52514461_52514462insG GRCh38
NC_000016.9:g.52548373_52548374insG , CM000678.1:g.52548373_52548374insG GRCh37
NC_000016.8:g.51105874_51105875insG NCBI36
NG_012623.1:g.38341_38342insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000219746.14:c.87+32175_87+32176insC MANE Select ENSP00000219746.9:n.87+32175_87+32176insC
ENST00000219746.13:c.87+32175_87+32176insC ENSP00000219746.9:n.87+32175_87+32176insC
ENST00000407228.7:c.75+4944_75+4945insC ENSP00000385705.3:n.75+4944_75+4945insC
ENST00000563091.1:c.-22+32906_-22+32907insC ENSP00000457401.1:n.-22+32906_-22+32907insC
ENST00000568436.1:c.87+32175_87+32176insC ENSP00000463843.1:n.87+32175_87+32176insC
NM_001080430.2:c.87+32175_87+32176insC NP_001073899.2:n.87+32175_87+32176insC
NM_001146188.1:c.75+4944_75+4945insC NP_001139660.1:n.75+4944_75+4945insC
XM_005255892.2:c.87+32175_87+32176insC XP_005255949.1:n.87+32175_87+32176insC
XM_005255893.2:c.75+4944_75+4945insC XP_005255950.1:n.75+4944_75+4945insC
NM_001080430.3:c.87+32175_87+32176insC NP_001073899.2:n.87+32175_87+32176insC
NM_001146188.2:c.75+4944_75+4945insC NP_001139660.1:n.75+4944_75+4945insC
XM_005255892.3:c.87+32175_87+32176insC XP_005255949.1:n.87+32175_87+32176insC
XM_017023142.1:c.75+4944_75+4945insC XP_016878631.1:n.75+4944_75+4945insC
XM_024450230.1:c.75+4944_75+4945insC XP_024305998.1:n.75+4944_75+4945insC
NM_001080430.4:c.87+32175_87+32176insC MANE Select NP_001073899.2:n.87+32175_87+32176insC