Canonical Allele Identifier: CA2222790971
Gene: TOX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52542321T= , CM000678.2:g.52542321T= GRCh38
NC_000016.9:g.52576233T= , CM000678.1:g.52576233T= GRCh37
NC_000016.8:g.51133734T= NCBI36
NG_012623.1:g.10482A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000219746.14:c.87+4316A= MANE Select ENSP00000219746.9:n.87+4316A=
ENST00000219746.13:c.87+4316A= ENSP00000219746.9:n.87+4316A=
ENST00000407228.7:c.-100+5393A= ENSP00000385705.3:n.-100+5393A=
ENST00000563091.1:c.-22+5047A= ENSP00000457401.1:n.-22+5047A=
ENST00000568436.1:c.87+4316A= ENSP00000463843.1:n.87+4316A=
NM_001080430.2:c.87+4316A= NP_001073899.2:n.87+4316A=
NM_001146188.1:c.-100+5393A= NP_001139660.1:n.-100+5393A=
XM_005255892.2:c.87+4316A= XP_005255949.1:n.87+4316A=
XM_005255893.2:c.-100+4316A= XP_005255950.1:n.-100+4316A=
NM_001080430.3:c.87+4316A= NP_001073899.2:n.87+4316A=
NM_001146188.2:c.-100+5393A= NP_001139660.1:n.-100+5393A=
XM_005255892.3:c.87+4316A= XP_005255949.1:n.87+4316A=
NM_001080430.4:c.87+4316A= MANE Select NP_001073899.2:n.87+4316A=