Canonical Allele Identifier: CA466790005

Gene: TNC

Linked Data

• MyVariant Identifiers: chr9:g.117797498C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035219C>G , CM000671.2:g.115035219C>G	GRCh38
NC_000009.11:g.117797498C>G , CM000671.1:g.117797498C>G	GRCh37
NC_000009.10:g.116837319C>G	NCBI36
NG_029637.1:g.88039G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000537320.6:c.3861G>C	ENSP00000443478.1:p.Val1287=
ENST00000542877.6:c.4683G>C	ENSP00000442242.1:p.Val1561=
ENST00000705190.1:c.2715G>C	ENSP00000516083.1:p.Val905=
ENST00000705191.1:c.1371G>C	ENSP00000516084.1:p.Val457=
ENST00000705192.1:c.4730G>C
ENST00000350763.9:c.5772G>C MANE Select	ENSP00000265131.4:p.Val1924=
ENST00000341037.8:c.5226G>C	ENSP00000339553.4:p.Val1742=
ENST00000350763.8:c.5772G>C	ENSP00000265131.4:p.Val1924=
ENST00000423613.6:c.4953G>C	ENSP00000411406.2:p.Val1651=
ENST00000460345.1:n.354G>C
ENST00000535648.5:c.4683G>C	ENSP00000438152.2:p.Val1561=
ENST00000537320.5:c.3861G>C	ENSP00000443478.1:p.Val1287=
ENST00000542877.5:c.4683G>C	ENSP00000442242.1:p.Val1561=
ENST00000544972.1:c.1459G>C
NM_002160.3:c.5772G>C	NP_002151.2:p.Val1924=
XM_005251972.2:c.5499G>C	XP_005252029.1:p.Val1833=
XM_005251973.2:c.4680G>C	XP_005252030.1:p.Val1560=
XM_005251974.2:c.4134G>C	XP_005252031.1:p.Val1378=
XM_005251975.2:c.3861G>C	XP_005252032.1:p.Val1287=
XM_006717096.2:c.6048G>C	XP_006717159.1:p.Val2016=
XM_006717097.2:c.5499G>C	XP_006717160.1:p.Val1833=
XM_006717098.2:c.5226G>C	XP_006717161.1:p.Val1742=
XM_006717100.2:c.4953G>C	XP_006717163.1:p.Val1651=
XM_006717101.2:c.4134G>C	XP_006717164.1:p.Val1378=
XM_011518622.1:c.5775G>C	XP_011516924.1:p.Val1925=
XM_011518623.1:c.5775G>C	XP_011516925.1:p.Val1925=
XM_011518624.1:c.5229G>C	XP_011516926.1:p.Val1743=
XM_011518625.1:c.5226G>C	XP_011516927.1:p.Val1742=
XM_011518626.1:c.4956G>C	XP_011516928.1:p.Val1652=
XM_011518627.1:c.4683G>C	XP_011516929.1:p.Val1561=
XM_011518628.1:c.4407G>C	XP_011516930.1:p.Val1469=
XM_011518629.1:c.4407G>C	XP_011516931.1:p.Val1469=
XM_005251972.4:c.5499G>C	XP_005252029.1:p.Val1833=
XM_005251973.4:c.4680G>C	XP_005252030.1:p.Val1560=
XM_005251974.4:c.4134G>C	XP_005252031.1:p.Val1378=
XM_005251975.4:c.3861G>C	XP_005252032.1:p.Val1287=
XM_006717096.4:c.6048G>C	XP_006717159.1:p.Val2016=
XM_006717097.4:c.5499G>C	XP_006717160.1:p.Val1833=
XM_006717098.4:c.5226G>C	XP_006717161.1:p.Val1742=
XM_006717101.4:c.4134G>C	XP_006717164.1:p.Val1378=
XM_011518625.3:c.5226G>C	XP_011516927.1:p.Val1742=
XM_011518626.3:c.4956G>C	XP_011516928.1:p.Val1652=
XM_011518628.3:c.4407G>C	XP_011516930.1:p.Val1469=
XM_011518629.3:c.4407G>C	XP_011516931.1:p.Val1469=
XM_017014678.2:c.6321G>C	XP_016870167.1:p.Val2107=
XM_017014679.2:c.6048G>C	XP_016870168.1:p.Val2016=
XM_017014680.2:c.6045G>C	XP_016870169.1:p.Val2015=
XM_017014681.2:c.5229G>C	XP_016870170.1:p.Val1743=
XM_024447530.1:c.6321G>C	XP_024303298.1:p.Val2107=
NM_002160.4:c.5772G>C MANE Select	NP_002151.2:p.Val1924=