Canonical Allele Identifier: CA1874113743

Gene: TNC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035248T= , CM000671.2:g.115035248T=	GRCh38
NC_000009.11:g.117797527T= , CM000671.1:g.117797527T=	GRCh37
NC_000009.10:g.116837348T=	NCBI36
NG_029637.1:g.88010A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537320.6:c.3832A=	ENSP00000443478.1:p.Thr1278=
ENST00000542877.6:c.4654A=	ENSP00000442242.1:p.Thr1552=
ENST00000705190.1:c.2686A=	ENSP00000516083.1:p.Thr896=
ENST00000705191.1:c.1342A=	ENSP00000516084.1:p.Thr448=
ENST00000705192.1:c.4701A=
ENST00000350763.9:c.5743A= MANE Select	ENSP00000265131.4:p.Thr1915=
ENST00000341037.8:c.5197A=	ENSP00000339553.4:p.Thr1733=
ENST00000350763.8:c.5743A=	ENSP00000265131.4:p.Thr1915=
ENST00000423613.6:c.4924A=	ENSP00000411406.2:p.Thr1642=
ENST00000460345.1:n.325A=
ENST00000535648.5:c.4654A=	ENSP00000438152.2:p.Thr1552=
ENST00000537320.5:c.3832A=	ENSP00000443478.1:p.Thr1278=
ENST00000542877.5:c.4654A=	ENSP00000442242.1:p.Thr1552=
ENST00000544972.1:c.1430A=
NM_002160.3:c.5743A=	NP_002151.2:p.Thr1915=
XM_005251972.2:c.5470A=	XP_005252029.1:p.Thr1824=
XM_005251973.2:c.4651A=	XP_005252030.1:p.Thr1551=
XM_005251974.2:c.4105A=	XP_005252031.1:p.Thr1369=
XM_005251975.2:c.3832A=	XP_005252032.1:p.Thr1278=
XM_006717096.2:c.6019A=	XP_006717159.1:p.Thr2007=
XM_006717097.2:c.5470A=	XP_006717160.1:p.Thr1824=
XM_006717098.2:c.5197A=	XP_006717161.1:p.Thr1733=
XM_006717100.2:c.4924A=	XP_006717163.1:p.Thr1642=
XM_006717101.2:c.4105A=	XP_006717164.1:p.Thr1369=
XM_011518622.1:c.5746A=	XP_011516924.1:p.Thr1916=
XM_011518623.1:c.5746A=	XP_011516925.1:p.Thr1916=
XM_011518624.1:c.5200A=	XP_011516926.1:p.Thr1734=
XM_011518625.1:c.5197A=	XP_011516927.1:p.Thr1733=
XM_011518626.1:c.4927A=	XP_011516928.1:p.Thr1643=
XM_011518627.1:c.4654A=	XP_011516929.1:p.Thr1552=
XM_011518628.1:c.4378A=	XP_011516930.1:p.Thr1460=
XM_011518629.1:c.4378A=	XP_011516931.1:p.Thr1460=
XM_005251972.4:c.5470A=	XP_005252029.1:p.Thr1824=
XM_005251973.4:c.4651A=	XP_005252030.1:p.Thr1551=
XM_005251974.4:c.4105A=	XP_005252031.1:p.Thr1369=
XM_005251975.4:c.3832A=	XP_005252032.1:p.Thr1278=
XM_006717096.4:c.6019A=	XP_006717159.1:p.Thr2007=
XM_006717097.4:c.5470A=	XP_006717160.1:p.Thr1824=
XM_006717098.4:c.5197A=	XP_006717161.1:p.Thr1733=
XM_006717101.4:c.4105A=	XP_006717164.1:p.Thr1369=
XM_011518625.3:c.5197A=	XP_011516927.1:p.Thr1733=
XM_011518626.3:c.4927A=	XP_011516928.1:p.Thr1643=
XM_011518628.3:c.4378A=	XP_011516930.1:p.Thr1460=
XM_011518629.3:c.4378A=	XP_011516931.1:p.Thr1460=
XM_017014678.2:c.6292A=	XP_016870167.1:p.Thr2098=
XM_017014679.2:c.6019A=	XP_016870168.1:p.Thr2007=
XM_017014680.2:c.6016A=	XP_016870169.1:p.Thr2006=
XM_017014681.2:c.5200A=	XP_016870170.1:p.Thr1734=
XM_024447530.1:c.6292A=	XP_024303298.1:p.Thr2098=
NM_002160.4:c.5743A= MANE Select	NP_002151.2:p.Thr1915=