Canonical Allele Identifier: CA2222759955
Gene: TOX3 HGNC NCBI

Linked Data

dbSNP Id: rs1962390454

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52514464_52514465insCTATTGGAGTTTGATAGCTAATTACAGAAC , CM000678.2:g.52514464_52514465insCTATTGGAGTTTGATAGCTAATTACAGAAC GRCh38
NC_000016.9:g.52548376_52548377insCTATTGGAGTTTGATAGCTAATTACAGAAC , CM000678.1:g.52548376_52548377insCTATTGGAGTTTGATAGCTAATTACAGAAC GRCh37
NC_000016.8:g.51105877_51105878insCTATTGGAGTTTGATAGCTAATTACAGAAC NCBI36
NG_012623.1:g.38340_38341insTCTGTAATTAGCTATCAAACTCCAATAGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000219746.14:c.87+32174_87+32175insTCTGTAATTAGCTATCAAACTCCAATAGGT MANE Select ENSP00000219746.9:n.87+32174_87+32175insTCTGTAATTAGCTATCAAACT...
ENST00000219746.13:c.87+32174_87+32175insTCTGTAATTAGCTATCAAACTCCAATAGGT ENSP00000219746.9:n.87+32174_87+32175insTCTGTAATTAGCTATCAAACT...
ENST00000407228.7:c.75+4943_75+4944insTCTGTAATTAGCTATCAAACTCCAATAGGT ENSP00000385705.3:n.75+4943_75+4944insTCTGTAATTAGCTATCAAACTCC...
ENST00000563091.1:c.-22+32905_-22+32906insTCTGTAATTAGCTATCAAACTCCAATAGGT ENSP00000457401.1:n.-22+32905_-22+32906insTCTGTAATTAGCTATCAAA...
ENST00000568436.1:c.87+32174_87+32175insTCTGTAATTAGCTATCAAACTCCAATAGGT ENSP00000463843.1:n.87+32174_87+32175insTCTGTAATTAGCTATCAAACT...
NM_001080430.2:c.87+32174_87+32175insTCTGTAATTAGCTATCAAACTCCAATAGGT NP_001073899.2:n.87+32174_87+32175insTCTGTAATTAGCTATCAAACTCCA...
NM_001146188.1:c.75+4943_75+4944insTCTGTAATTAGCTATCAAACTCCAATAGGT NP_001139660.1:n.75+4943_75+4944insTCTGTAATTAGCTATCAAACTCCAAT...
XM_005255892.2:c.87+32174_87+32175insTCTGTAATTAGCTATCAAACTCCAATAGGT XP_005255949.1:n.87+32174_87+32175insTCTGTAATTAGCTATCAAACTCCA...
XM_005255893.2:c.75+4943_75+4944insTCTGTAATTAGCTATCAAACTCCAATAGGT XP_005255950.1:n.75+4943_75+4944insTCTGTAATTAGCTATCAAACTCCAAT...
NM_001080430.3:c.87+32174_87+32175insTCTGTAATTAGCTATCAAACTCCAATAGGT NP_001073899.2:n.87+32174_87+32175insTCTGTAATTAGCTATCAAACTCCA...
NM_001146188.2:c.75+4943_75+4944insTCTGTAATTAGCTATCAAACTCCAATAGGT NP_001139660.1:n.75+4943_75+4944insTCTGTAATTAGCTATCAAACTCCAAT...
XM_005255892.3:c.87+32174_87+32175insTCTGTAATTAGCTATCAAACTCCAATAGGT XP_005255949.1:n.87+32174_87+32175insTCTGTAATTAGCTATCAAACTCCA...
XM_017023142.1:c.75+4943_75+4944insTCTGTAATTAGCTATCAAACTCCAATAGGT XP_016878631.1:n.75+4943_75+4944insTCTGTAATTAGCTATCAAACTCCAAT...
XM_024450230.1:c.75+4943_75+4944insTCTGTAATTAGCTATCAAACTCCAATAGGT XP_024305998.1:n.75+4943_75+4944insTCTGTAATTAGCTATCAAACTCCAAT...
NM_001080430.4:c.87+32174_87+32175insTCTGTAATTAGCTATCAAACTCCAATAGGT MANE Select NP_001073899.2:n.87+32174_87+32175insTCTGTAATTAGCTATCAAACTCCA...