Canonical Allele Identifier: CA466790285

Gene: TNC

Linked Data

• MyVariant Identifiers: chr9:g.117797576A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035297A>T , CM000671.2:g.115035297A>T	GRCh38
NC_000009.11:g.117797576A>T , CM000671.1:g.117797576A>T	GRCh37
NC_000009.10:g.116837397A>T	NCBI36
NG_029637.1:g.87961T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537320.6:c.3783T>A	ENSP00000443478.1:p.Val1261=
ENST00000542877.6:c.4605T>A	ENSP00000442242.1:p.Val1535=
ENST00000705190.1:c.2637T>A	ENSP00000516083.1:p.Val879=
ENST00000705191.1:c.1293T>A	ENSP00000516084.1:p.Val431=
ENST00000705192.1:c.4652T>A
ENST00000350763.9:c.5694T>A MANE Select	ENSP00000265131.4:p.Val1898=
ENST00000341037.8:c.5148T>A	ENSP00000339553.4:p.Val1716=
ENST00000350763.8:c.5694T>A	ENSP00000265131.4:p.Val1898=
ENST00000423613.6:c.4875T>A	ENSP00000411406.2:p.Val1625=
ENST00000460345.1:n.276T>A
ENST00000535648.5:c.4605T>A	ENSP00000438152.2:p.Val1535=
ENST00000537320.5:c.3783T>A	ENSP00000443478.1:p.Val1261=
ENST00000542877.5:c.4605T>A	ENSP00000442242.1:p.Val1535=
ENST00000544972.1:c.1381T>A
NM_002160.3:c.5694T>A	NP_002151.2:p.Val1898=
XM_005251972.2:c.5421T>A	XP_005252029.1:p.Val1807=
XM_005251973.2:c.4602T>A	XP_005252030.1:p.Val1534=
XM_005251974.2:c.4056T>A	XP_005252031.1:p.Val1352=
XM_005251975.2:c.3783T>A	XP_005252032.1:p.Val1261=
XM_006717096.2:c.5970T>A	XP_006717159.1:p.Val1990=
XM_006717097.2:c.5421T>A	XP_006717160.1:p.Val1807=
XM_006717098.2:c.5148T>A	XP_006717161.1:p.Val1716=
XM_006717100.2:c.4875T>A	XP_006717163.1:p.Val1625=
XM_006717101.2:c.4056T>A	XP_006717164.1:p.Val1352=
XM_011518622.1:c.5697T>A	XP_011516924.1:p.Val1899=
XM_011518623.1:c.5697T>A	XP_011516925.1:p.Val1899=
XM_011518624.1:c.5151T>A	XP_011516926.1:p.Val1717=
XM_011518625.1:c.5148T>A	XP_011516927.1:p.Val1716=
XM_011518626.1:c.4878T>A	XP_011516928.1:p.Val1626=
XM_011518627.1:c.4605T>A	XP_011516929.1:p.Val1535=
XM_011518628.1:c.4329T>A	XP_011516930.1:p.Val1443=
XM_011518629.1:c.4329T>A	XP_011516931.1:p.Val1443=
XM_005251972.4:c.5421T>A	XP_005252029.1:p.Val1807=
XM_005251973.4:c.4602T>A	XP_005252030.1:p.Val1534=
XM_005251974.4:c.4056T>A	XP_005252031.1:p.Val1352=
XM_005251975.4:c.3783T>A	XP_005252032.1:p.Val1261=
XM_006717096.4:c.5970T>A	XP_006717159.1:p.Val1990=
XM_006717097.4:c.5421T>A	XP_006717160.1:p.Val1807=
XM_006717098.4:c.5148T>A	XP_006717161.1:p.Val1716=
XM_006717101.4:c.4056T>A	XP_006717164.1:p.Val1352=
XM_011518625.3:c.5148T>A	XP_011516927.1:p.Val1716=
XM_011518626.3:c.4878T>A	XP_011516928.1:p.Val1626=
XM_011518628.3:c.4329T>A	XP_011516930.1:p.Val1443=
XM_011518629.3:c.4329T>A	XP_011516931.1:p.Val1443=
XM_017014678.2:c.6243T>A	XP_016870167.1:p.Val2081=
XM_017014679.2:c.5970T>A	XP_016870168.1:p.Val1990=
XM_017014680.2:c.5967T>A	XP_016870169.1:p.Val1989=
XM_017014681.2:c.5151T>A	XP_016870170.1:p.Val1717=
XM_024447530.1:c.6243T>A	XP_024303298.1:p.Val2081=
NM_002160.4:c.5694T>A MANE Select	NP_002151.2:p.Val1898=