Canonical Allele Identifier: CA2222759768
Gene: TOX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52514300_52514301delinsTG , CM000678.2:g.52514300_52514301delinsTG GRCh38
NC_000016.9:g.52548212_52548213delinsTG , CM000678.1:g.52548212_52548213delinsTG GRCh37
NC_000016.8:g.51105713_51105714delinsTG NCBI36
NG_012623.1:g.38502_38503delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000219746.14:c.87+32336_87+32337delinsCA MANE Select ENSP00000219746.9:n.87+32336_87+32337delinsCA
ENST00000219746.13:c.87+32336_87+32337delinsCA ENSP00000219746.9:n.87+32336_87+32337delinsCA
ENST00000407228.7:c.75+5105_75+5106delinsCA ENSP00000385705.3:n.75+5105_75+5106delinsCA
ENST00000563091.1:c.-22+33067_-22+33068delinsCA ENSP00000457401.1:n.-22+33067_-22+33068delinsCA
ENST00000568436.1:c.87+32336_87+32337delinsCA ENSP00000463843.1:n.87+32336_87+32337delinsCA
NM_001080430.2:c.87+32336_87+32337delinsCA NP_001073899.2:n.87+32336_87+32337delinsCA
NM_001146188.1:c.75+5105_75+5106delinsCA NP_001139660.1:n.75+5105_75+5106delinsCA
XM_005255892.2:c.87+32336_87+32337delinsCA XP_005255949.1:n.87+32336_87+32337delinsCA
XM_005255893.2:c.75+5105_75+5106delinsCA XP_005255950.1:n.75+5105_75+5106delinsCA
NM_001080430.3:c.87+32336_87+32337delinsCA NP_001073899.2:n.87+32336_87+32337delinsCA
NM_001146188.2:c.75+5105_75+5106delinsCA NP_001139660.1:n.75+5105_75+5106delinsCA
XM_005255892.3:c.87+32336_87+32337delinsCA XP_005255949.1:n.87+32336_87+32337delinsCA
XM_017023142.1:c.75+5105_75+5106delinsCA XP_016878631.1:n.75+5105_75+5106delinsCA
XM_024450230.1:c.75+5105_75+5106delinsCA XP_024305998.1:n.75+5105_75+5106delinsCA
NM_001080430.4:c.87+32336_87+32337delinsCA MANE Select NP_001073899.2:n.87+32336_87+32337delinsCA