Canonical Allele Identifier: CA2222752918

Gene: TOX3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.52500255T>G , CM000678.2:g.52500255T>G	GRCh38
NC_000016.9:g.52534167T>G , CM000678.1:g.52534167T>G	GRCh37
NC_000016.8:g.51091668T>G	NCBI36
NG_012623.1:g.52548A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219746.14:c.88-31681A>C MANE Select	ENSP00000219746.9:n.88-31681A>C
ENST00000219746.13:c.88-31681A>C	ENSP00000219746.9:n.88-31681A>C
ENST00000407228.7:c.75+19151A>C	ENSP00000385705.3:n.75+19151A>C
ENST00000563091.1:c.-21-31681A>C	ENSP00000457401.1:n.-21-31681A>C
ENST00000568436.1:c.88-24615A>C	ENSP00000463843.1:n.88-24615A>C
NM_001080430.2:c.88-31681A>C	NP_001073899.2:n.88-31681A>C
NM_001146188.1:c.75+19151A>C	NP_001139660.1:n.75+19151A>C
XM_005255892.2:c.88-31681A>C	XP_005255949.1:n.88-31681A>C
XM_005255893.2:c.75+19151A>C	XP_005255950.1:n.75+19151A>C
NM_001080430.3:c.88-31681A>C	NP_001073899.2:n.88-31681A>C
NM_001146188.2:c.75+19151A>C	NP_001139660.1:n.75+19151A>C
XM_005255892.3:c.88-31681A>C	XP_005255949.1:n.88-31681A>C
XM_017023142.1:c.75+19151A>C	XP_016878631.1:n.75+19151A>C
XM_024450230.1:c.75+19151A>C	XP_024305998.1:n.75+19151A>C
NM_001080430.4:c.88-31681A>C MANE Select	NP_001073899.2:n.88-31681A>C