Canonical Allele Identifier: CA2222790816

Gene: TOX3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.52542110A= , CM000678.2:g.52542110A=	GRCh38
NC_000016.9:g.52576022A= , CM000678.1:g.52576022A=	GRCh37
NC_000016.8:g.51133523A=	NCBI36
NG_012623.1:g.10693T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219746.14:c.87+4527T= MANE Select	ENSP00000219746.9:n.87+4527T=
ENST00000219746.13:c.87+4527T=	ENSP00000219746.9:n.87+4527T=
ENST00000407228.7:c.-100+5604T=	ENSP00000385705.3:n.-100+5604T=
ENST00000563091.1:c.-22+5258T=	ENSP00000457401.1:n.-22+5258T=
ENST00000568436.1:c.87+4527T=	ENSP00000463843.1:n.87+4527T=
NM_001080430.2:c.87+4527T=	NP_001073899.2:n.87+4527T=
NM_001146188.1:c.-100+5604T=	NP_001139660.1:n.-100+5604T=
XM_005255892.2:c.87+4527T=	XP_005255949.1:n.87+4527T=
XM_005255893.2:c.-100+4527T=	XP_005255950.1:n.-100+4527T=
NM_001080430.3:c.87+4527T=	NP_001073899.2:n.87+4527T=
NM_001146188.2:c.-100+5604T=	NP_001139660.1:n.-100+5604T=
XM_005255892.3:c.87+4527T=	XP_005255949.1:n.87+4527T=
NM_001080430.4:c.87+4527T= MANE Select	NP_001073899.2:n.87+4527T=