Canonical Allele Identifier: CA5207540

Gene: TNC

Linked Data

• dbSNP Id: rs770685046
• ExAC: 9:117797502 G / A
• gnomAD v2: 9-117797502-G-A
• gnomAD v4: 9-115035223-G-A
• COSMIC: COSM1701564
• MyVariant Identifiers: chr9:g.117797502G>A (hg19) ; chr9:g.115035223G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035223G>A , CM000671.2:g.115035223G>A	GRCh38
NC_000009.11:g.117797502G>A , CM000671.1:g.117797502G>A	GRCh37
NC_000009.10:g.116837323G>A	NCBI36
NG_029637.1:g.88035C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000537320.6:c.3857C>T	ENSP00000443478.1:p.Ser1286Leu
ENST00000542877.6:c.4679C>T	ENSP00000442242.1:p.Ser1560Leu
ENST00000705190.1:c.2711C>T	ENSP00000516083.1:p.Ser904Leu
ENST00000705191.1:c.1367C>T	ENSP00000516084.1:p.Ser456Leu
ENST00000705192.1:c.4726C>T
ENST00000350763.9:c.5768C>T MANE Select	ENSP00000265131.4:p.Ser1923Leu
ENST00000341037.8:c.5222C>T	ENSP00000339553.4:p.Ser1741Leu
ENST00000350763.8:c.5768C>T	ENSP00000265131.4:p.Ser1923Leu
ENST00000423613.6:c.4949C>T	ENSP00000411406.2:p.Ser1650Leu
ENST00000460345.1:n.350C>T
ENST00000535648.5:c.4679C>T	ENSP00000438152.2:p.Ser1560Leu
ENST00000537320.5:c.3857C>T	ENSP00000443478.1:p.Ser1286Leu
ENST00000542877.5:c.4679C>T	ENSP00000442242.1:p.Ser1560Leu
ENST00000544972.1:c.1455C>T
NM_002160.3:c.5768C>T	NP_002151.2:p.Ser1923Leu
XM_005251972.2:c.5495C>T	XP_005252029.1:p.Ser1832Leu
XM_005251973.2:c.4676C>T	XP_005252030.1:p.Ser1559Leu
XM_005251974.2:c.4130C>T	XP_005252031.1:p.Ser1377Leu
XM_005251975.2:c.3857C>T	XP_005252032.1:p.Ser1286Leu
XM_006717096.2:c.6044C>T	XP_006717159.1:p.Ser2015Leu
XM_006717097.2:c.5495C>T	XP_006717160.1:p.Ser1832Leu
XM_006717098.2:c.5222C>T	XP_006717161.1:p.Ser1741Leu
XM_006717100.2:c.4949C>T	XP_006717163.1:p.Ser1650Leu
XM_006717101.2:c.4130C>T	XP_006717164.1:p.Ser1377Leu
XM_011518622.1:c.5771C>T	XP_011516924.1:p.Ser1924Leu
XM_011518623.1:c.5771C>T	XP_011516925.1:p.Ser1924Leu
XM_011518624.1:c.5225C>T	XP_011516926.1:p.Ser1742Leu
XM_011518625.1:c.5222C>T	XP_011516927.1:p.Ser1741Leu
XM_011518626.1:c.4952C>T	XP_011516928.1:p.Ser1651Leu
XM_011518627.1:c.4679C>T	XP_011516929.1:p.Ser1560Leu
XM_011518628.1:c.4403C>T	XP_011516930.1:p.Ser1468Leu
XM_011518629.1:c.4403C>T	XP_011516931.1:p.Ser1468Leu
XM_005251972.4:c.5495C>T	XP_005252029.1:p.Ser1832Leu
XM_005251973.4:c.4676C>T	XP_005252030.1:p.Ser1559Leu
XM_005251974.4:c.4130C>T	XP_005252031.1:p.Ser1377Leu
XM_005251975.4:c.3857C>T	XP_005252032.1:p.Ser1286Leu
XM_006717096.4:c.6044C>T	XP_006717159.1:p.Ser2015Leu
XM_006717097.4:c.5495C>T	XP_006717160.1:p.Ser1832Leu
XM_006717098.4:c.5222C>T	XP_006717161.1:p.Ser1741Leu
XM_006717101.4:c.4130C>T	XP_006717164.1:p.Ser1377Leu
XM_011518625.3:c.5222C>T	XP_011516927.1:p.Ser1741Leu
XM_011518626.3:c.4952C>T	XP_011516928.1:p.Ser1651Leu
XM_011518628.3:c.4403C>T	XP_011516930.1:p.Ser1468Leu
XM_011518629.3:c.4403C>T	XP_011516931.1:p.Ser1468Leu
XM_017014678.2:c.6317C>T	XP_016870167.1:p.Ser2106Leu
XM_017014679.2:c.6044C>T	XP_016870168.1:p.Ser2015Leu
XM_017014680.2:c.6041C>T	XP_016870169.1:p.Ser2014Leu
XM_017014681.2:c.5225C>T	XP_016870170.1:p.Ser1742Leu
XM_024447530.1:c.6317C>T	XP_024303298.1:p.Ser2106Leu
NM_002160.4:c.5768C>T MANE Select	NP_002151.2:p.Ser1923Leu