Canonical Allele Identifier: CA919707577

Gene: TOX3

Linked Data

• dbSNP Id: rs1567358528

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.52542250del , CM000678.2:g.52542250del	GRCh38
NC_000016.9:g.52576162del , CM000678.1:g.52576162del	GRCh37
NC_000016.8:g.51133663del	NCBI36
NG_012623.1:g.10554del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219746.14:c.87+4388del MANE Select	ENSP00000219746.9:n.87+4388del
ENST00000219746.13:c.87+4388del	ENSP00000219746.9:n.87+4388del
ENST00000407228.7:c.-100+5465del	ENSP00000385705.3:n.-100+5465del
ENST00000563091.1:c.-22+5119del	ENSP00000457401.1:n.-22+5119del
ENST00000568436.1:c.87+4388del	ENSP00000463843.1:n.87+4388del
NM_001080430.2:c.87+4388del	NP_001073899.2:n.87+4388del
NM_001146188.1:c.-100+5465del	NP_001139660.1:n.-100+5465del
XM_005255892.2:c.87+4388del	XP_005255949.1:n.87+4388del
XM_005255893.2:c.-100+4388del	XP_005255950.1:n.-100+4388del
NM_001080430.3:c.87+4388del	NP_001073899.2:n.87+4388del
NM_001146188.2:c.-100+5465del	NP_001139660.1:n.-100+5465del
XM_005255892.3:c.87+4388del	XP_005255949.1:n.87+4388del
NM_001080430.4:c.87+4388del MANE Select	NP_001073899.2:n.87+4388del