Canonical Allele Identifier: CA2222759913
Gene: TOX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52514437_52514438delinsTA , CM000678.2:g.52514437_52514438delinsTA GRCh38
NC_000016.9:g.52548349_52548350delinsTA , CM000678.1:g.52548349_52548350delinsTA GRCh37
NC_000016.8:g.51105850_51105851delinsTA NCBI36
NG_012623.1:g.38365_38366delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000219746.14:c.87+32199_87+32200delinsTA MANE Select ENSP00000219746.9:n.87+32199_87+32200delinsTA
ENST00000219746.13:c.87+32199_87+32200delinsTA ENSP00000219746.9:n.87+32199_87+32200delinsTA
ENST00000407228.7:c.75+4968_75+4969delinsTA ENSP00000385705.3:n.75+4968_75+4969delinsTA
ENST00000563091.1:c.-22+32930_-22+32931delinsTA ENSP00000457401.1:n.-22+32930_-22+32931delinsTA
ENST00000568436.1:c.87+32199_87+32200delinsTA ENSP00000463843.1:n.87+32199_87+32200delinsTA
NM_001080430.2:c.87+32199_87+32200delinsTA NP_001073899.2:n.87+32199_87+32200delinsTA
NM_001146188.1:c.75+4968_75+4969delinsTA NP_001139660.1:n.75+4968_75+4969delinsTA
XM_005255892.2:c.87+32199_87+32200delinsTA XP_005255949.1:n.87+32199_87+32200delinsTA
XM_005255893.2:c.75+4968_75+4969delinsTA XP_005255950.1:n.75+4968_75+4969delinsTA
NM_001080430.3:c.87+32199_87+32200delinsTA NP_001073899.2:n.87+32199_87+32200delinsTA
NM_001146188.2:c.75+4968_75+4969delinsTA NP_001139660.1:n.75+4968_75+4969delinsTA
XM_005255892.3:c.87+32199_87+32200delinsTA XP_005255949.1:n.87+32199_87+32200delinsTA
XM_017023142.1:c.75+4968_75+4969delinsTA XP_016878631.1:n.75+4968_75+4969delinsTA
XM_024450230.1:c.75+4968_75+4969delinsTA XP_024305998.1:n.75+4968_75+4969delinsTA
NM_001080430.4:c.87+32199_87+32200delinsTA MANE Select NP_001073899.2:n.87+32199_87+32200delinsTA