Canonical Allele Identifier: CA658773192

Gene: TNC

Linked Data

• PubMed: PMID:28263302

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115046526dup , CM000671.2:g.115046526dup	GRCh38
NC_000009.11:g.117808805dup , CM000671.1:g.117808805dup	GRCh37
NC_000009.10:g.116848626dup	NCBI36
NG_029637.1:g.76736dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476680.2:c.318-4181dup
ENST00000537320.6:c.3215-4181dup	ENSP00000443478.1:n.3215-4181dup
ENST00000542877.6:c.3924dup	ENSP00000442242.1:p.Glu1309ArgfsTer14
ENST00000705190.1:c.1956dup	ENSP00000516083.1:p.Glu653ArgfsTer14
ENST00000705191.1:c.612dup	ENSP00000516084.1:p.Glu205ArgfsTer14
ENST00000705192.1:c.3971dup
ENST00000350763.9:c.5013dup MANE Select	ENSP00000265131.4:p.Glu1672ArgfsTer14
ENST00000341037.8:c.4467dup	ENSP00000339553.4:p.Glu1490ArgfsTer14
ENST00000350763.8:c.5013dup	ENSP00000265131.4:p.Glu1672ArgfsTer14
ENST00000423613.6:c.4307-4181dup	ENSP00000411406.2:n.4307-4181dup
ENST00000473855.1:n.331dup
ENST00000476680.1:n.253-4181dup
ENST00000498724.5:n.40-4181dup
ENST00000535648.5:c.3924dup	ENSP00000438152.2:p.Glu1309ArgfsTer14
ENST00000537320.5:c.3215-4181dup	ENSP00000443478.1:n.3215-4181dup
ENST00000542877.5:c.3924dup	ENSP00000442242.1:p.Glu1309ArgfsTer14
ENST00000544972.1:c.700dup
NM_002160.3:c.5013dup	NP_002151.2:p.Glu1672ArgfsTer14
XM_005251972.2:c.4740dup	XP_005252029.1:p.Glu1581ArgfsTer14
XM_005251973.2:c.4034-4181dup	XP_005252030.1:n.4034-4181dup
XM_005251974.2:c.3375dup	XP_005252031.1:p.Glu1126ArgfsTer14
XM_005251975.2:c.3215-4181dup	XP_005252032.1:n.3215-4181dup
XM_006717096.2:c.5289dup	XP_006717159.1:p.Glu1764ArgfsTer14
XM_006717097.2:c.4740dup	XP_006717160.1:p.Glu1581ArgfsTer14
XM_006717098.2:c.4467dup	XP_006717161.1:p.Glu1490ArgfsTer14
XM_006717100.2:c.4307-4181dup	XP_006717163.1:n.4307-4181dup
XM_006717101.2:c.3488-4181dup	XP_006717164.1:n.3488-4181dup
XM_011518622.1:c.5016dup	XP_011516924.1:p.Glu1673ArgfsTer14
XM_011518623.1:c.5016dup	XP_011516925.1:p.Glu1673ArgfsTer14
XM_011518624.1:c.4470dup	XP_011516926.1:p.Glu1491ArgfsTer14
XM_011518625.1:c.4580-4181dup	XP_011516927.1:n.4580-4181dup
XM_011518626.1:c.4197dup	XP_011516928.1:p.Glu1400ArgfsTer14
XM_011518627.1:c.3924dup	XP_011516929.1:p.Glu1309ArgfsTer14
XM_011518628.1:c.3761-4181dup	XP_011516930.1:n.3761-4181dup
XM_011518629.1:c.3648dup	XP_011516931.1:p.Glu1217ArgfsTer14
XM_005251972.4:c.4740dup	XP_005252029.1:p.Glu1581ArgfsTer14
XM_005251973.4:c.4034-4181dup	XP_005252030.1:n.4034-4181dup
XM_005251974.4:c.3375dup	XP_005252031.1:p.Glu1126ArgfsTer14
XM_005251975.4:c.3215-4181dup	XP_005252032.1:n.3215-4181dup
XM_006717096.4:c.5289dup	XP_006717159.1:p.Glu1764ArgfsTer14
XM_006717097.4:c.4740dup	XP_006717160.1:p.Glu1581ArgfsTer14
XM_006717098.4:c.4467dup	XP_006717161.1:p.Glu1490ArgfsTer14
XM_006717101.4:c.3488-4181dup	XP_006717164.1:n.3488-4181dup
XM_011518625.3:c.4580-4181dup	XP_011516927.1:n.4580-4181dup
XM_011518626.3:c.4197dup	XP_011516928.1:p.Glu1400ArgfsTer14
XM_011518628.3:c.3761-4181dup	XP_011516930.1:n.3761-4181dup
XM_011518629.3:c.3648dup	XP_011516931.1:p.Glu1217ArgfsTer14
XM_017014678.2:c.5562dup	XP_016870167.1:p.Glu1855ArgfsTer14
XM_017014679.2:c.5289dup	XP_016870168.1:p.Glu1764ArgfsTer14
XM_017014680.2:c.5286dup	XP_016870169.1:p.Glu1763ArgfsTer14
XM_017014681.2:c.4470dup	XP_016870170.1:p.Glu1491ArgfsTer14
XM_024447530.1:c.5562dup	XP_024303298.1:p.Glu1855ArgfsTer14
NM_002160.4:c.5013dup MANE Select	NP_002151.2:p.Glu1672ArgfsTer14