Canonical Allele Identifier: CA2222760020

Gene: TOX3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.52514504G= , CM000678.2:g.52514504G=	GRCh38
NC_000016.9:g.52548416G= , CM000678.1:g.52548416G=	GRCh37
NC_000016.8:g.51105917G=	NCBI36
NG_012623.1:g.38299C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219746.14:c.87+32133C= MANE Select	ENSP00000219746.9:n.87+32133C=
ENST00000219746.13:c.87+32133C=	ENSP00000219746.9:n.87+32133C=
ENST00000407228.7:c.75+4902C=	ENSP00000385705.3:n.75+4902C=
ENST00000563091.1:c.-22+32864C=	ENSP00000457401.1:n.-22+32864C=
ENST00000568436.1:c.87+32133C=	ENSP00000463843.1:n.87+32133C=
NM_001080430.2:c.87+32133C=	NP_001073899.2:n.87+32133C=
NM_001146188.1:c.75+4902C=	NP_001139660.1:n.75+4902C=
XM_005255892.2:c.87+32133C=	XP_005255949.1:n.87+32133C=
XM_005255893.2:c.75+4902C=	XP_005255950.1:n.75+4902C=
NM_001080430.3:c.87+32133C=	NP_001073899.2:n.87+32133C=
NM_001146188.2:c.75+4902C=	NP_001139660.1:n.75+4902C=
XM_005255892.3:c.87+32133C=	XP_005255949.1:n.87+32133C=
XM_017023142.1:c.75+4902C=	XP_016878631.1:n.75+4902C=
XM_024450230.1:c.75+4902C=	XP_024305998.1:n.75+4902C=
NM_001080430.4:c.87+32133C= MANE Select	NP_001073899.2:n.87+32133C=