Canonical Allele Identifier: CA374626429

Gene: TNC

Linked Data

• dbSNP Id: rs2131788641
• MyVariant Identifiers: chr9:g.117797500C>T (hg19) ; chr9:g.115035221C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035221C>T , CM000671.2:g.115035221C>T	GRCh38
NC_000009.11:g.117797500C>T , CM000671.1:g.117797500C>T	GRCh37
NC_000009.10:g.116837321C>T	NCBI36
NG_029637.1:g.88037G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000537320.6:c.3859G>A	ENSP00000443478.1:p.Val1287Met
ENST00000542877.6:c.4681G>A	ENSP00000442242.1:p.Val1561Met
ENST00000705190.1:c.2713G>A	ENSP00000516083.1:p.Val905Met
ENST00000705191.1:c.1369G>A	ENSP00000516084.1:p.Val457Met
ENST00000705192.1:c.4728G>A
ENST00000350763.9:c.5770G>A MANE Select	ENSP00000265131.4:p.Val1924Met
ENST00000341037.8:c.5224G>A	ENSP00000339553.4:p.Val1742Met
ENST00000350763.8:c.5770G>A	ENSP00000265131.4:p.Val1924Met
ENST00000423613.6:c.4951G>A	ENSP00000411406.2:p.Val1651Met
ENST00000460345.1:n.352G>A
ENST00000535648.5:c.4681G>A	ENSP00000438152.2:p.Val1561Met
ENST00000537320.5:c.3859G>A	ENSP00000443478.1:p.Val1287Met
ENST00000542877.5:c.4681G>A	ENSP00000442242.1:p.Val1561Met
ENST00000544972.1:c.1457G>A
NM_002160.3:c.5770G>A	NP_002151.2:p.Val1924Met
XM_005251972.2:c.5497G>A	XP_005252029.1:p.Val1833Met
XM_005251973.2:c.4678G>A	XP_005252030.1:p.Val1560Met
XM_005251974.2:c.4132G>A	XP_005252031.1:p.Val1378Met
XM_005251975.2:c.3859G>A	XP_005252032.1:p.Val1287Met
XM_006717096.2:c.6046G>A	XP_006717159.1:p.Val2016Met
XM_006717097.2:c.5497G>A	XP_006717160.1:p.Val1833Met
XM_006717098.2:c.5224G>A	XP_006717161.1:p.Val1742Met
XM_006717100.2:c.4951G>A	XP_006717163.1:p.Val1651Met
XM_006717101.2:c.4132G>A	XP_006717164.1:p.Val1378Met
XM_011518622.1:c.5773G>A	XP_011516924.1:p.Val1925Met
XM_011518623.1:c.5773G>A	XP_011516925.1:p.Val1925Met
XM_011518624.1:c.5227G>A	XP_011516926.1:p.Val1743Met
XM_011518625.1:c.5224G>A	XP_011516927.1:p.Val1742Met
XM_011518626.1:c.4954G>A	XP_011516928.1:p.Val1652Met
XM_011518627.1:c.4681G>A	XP_011516929.1:p.Val1561Met
XM_011518628.1:c.4405G>A	XP_011516930.1:p.Val1469Met
XM_011518629.1:c.4405G>A	XP_011516931.1:p.Val1469Met
XM_005251972.4:c.5497G>A	XP_005252029.1:p.Val1833Met
XM_005251973.4:c.4678G>A	XP_005252030.1:p.Val1560Met
XM_005251974.4:c.4132G>A	XP_005252031.1:p.Val1378Met
XM_005251975.4:c.3859G>A	XP_005252032.1:p.Val1287Met
XM_006717096.4:c.6046G>A	XP_006717159.1:p.Val2016Met
XM_006717097.4:c.5497G>A	XP_006717160.1:p.Val1833Met
XM_006717098.4:c.5224G>A	XP_006717161.1:p.Val1742Met
XM_006717101.4:c.4132G>A	XP_006717164.1:p.Val1378Met
XM_011518625.3:c.5224G>A	XP_011516927.1:p.Val1742Met
XM_011518626.3:c.4954G>A	XP_011516928.1:p.Val1652Met
XM_011518628.3:c.4405G>A	XP_011516930.1:p.Val1469Met
XM_011518629.3:c.4405G>A	XP_011516931.1:p.Val1469Met
XM_017014678.2:c.6319G>A	XP_016870167.1:p.Val2107Met
XM_017014679.2:c.6046G>A	XP_016870168.1:p.Val2016Met
XM_017014680.2:c.6043G>A	XP_016870169.1:p.Val2015Met
XM_017014681.2:c.5227G>A	XP_016870170.1:p.Val1743Met
XM_024447530.1:c.6319G>A	XP_024303298.1:p.Val2107Met
NM_002160.4:c.5770G>A MANE Select	NP_002151.2:p.Val1924Met