Canonical Allele Identifier: CA5207561

Gene: TNC

Linked Data

• dbSNP Id: rs775636762
• ExAC: 9:117797571 G / T
• gnomAD v2: 9-117797571-G-T
• gnomAD v4: 9-115035292-G-T
• MyVariant Identifiers: chr9:g.117797571G>T (hg19) ; chr9:g.115035292G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035292G>T , CM000671.2:g.115035292G>T	GRCh38
NC_000009.11:g.117797571G>T , CM000671.1:g.117797571G>T	GRCh37
NC_000009.10:g.116837392G>T	NCBI36
NG_029637.1:g.87966C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537320.6:c.3788C>A	ENSP00000443478.1:p.Ser1263Ter
ENST00000542877.6:c.4610C>A	ENSP00000442242.1:p.Ser1537Ter
ENST00000705190.1:c.2642C>A	ENSP00000516083.1:p.Ser881Ter
ENST00000705191.1:c.1298C>A	ENSP00000516084.1:p.Ser433Ter
ENST00000705192.1:c.4657C>A
ENST00000350763.9:c.5699C>A MANE Select	ENSP00000265131.4:p.Ser1900Ter
ENST00000341037.8:c.5153C>A	ENSP00000339553.4:p.Ser1718Ter
ENST00000350763.8:c.5699C>A	ENSP00000265131.4:p.Ser1900Ter
ENST00000423613.6:c.4880C>A	ENSP00000411406.2:p.Ser1627Ter
ENST00000460345.1:n.281C>A
ENST00000535648.5:c.4610C>A	ENSP00000438152.2:p.Ser1537Ter
ENST00000537320.5:c.3788C>A	ENSP00000443478.1:p.Ser1263Ter
ENST00000542877.5:c.4610C>A	ENSP00000442242.1:p.Ser1537Ter
ENST00000544972.1:c.1386C>A
NM_002160.3:c.5699C>A	NP_002151.2:p.Ser1900Ter
XM_005251972.2:c.5426C>A	XP_005252029.1:p.Ser1809Ter
XM_005251973.2:c.4607C>A	XP_005252030.1:p.Ser1536Ter
XM_005251974.2:c.4061C>A	XP_005252031.1:p.Ser1354Ter
XM_005251975.2:c.3788C>A	XP_005252032.1:p.Ser1263Ter
XM_006717096.2:c.5975C>A	XP_006717159.1:p.Ser1992Ter
XM_006717097.2:c.5426C>A	XP_006717160.1:p.Ser1809Ter
XM_006717098.2:c.5153C>A	XP_006717161.1:p.Ser1718Ter
XM_006717100.2:c.4880C>A	XP_006717163.1:p.Ser1627Ter
XM_006717101.2:c.4061C>A	XP_006717164.1:p.Ser1354Ter
XM_011518622.1:c.5702C>A	XP_011516924.1:p.Ser1901Ter
XM_011518623.1:c.5702C>A	XP_011516925.1:p.Ser1901Ter
XM_011518624.1:c.5156C>A	XP_011516926.1:p.Ser1719Ter
XM_011518625.1:c.5153C>A	XP_011516927.1:p.Ser1718Ter
XM_011518626.1:c.4883C>A	XP_011516928.1:p.Ser1628Ter
XM_011518627.1:c.4610C>A	XP_011516929.1:p.Ser1537Ter
XM_011518628.1:c.4334C>A	XP_011516930.1:p.Ser1445Ter
XM_011518629.1:c.4334C>A	XP_011516931.1:p.Ser1445Ter
XM_005251972.4:c.5426C>A	XP_005252029.1:p.Ser1809Ter
XM_005251973.4:c.4607C>A	XP_005252030.1:p.Ser1536Ter
XM_005251974.4:c.4061C>A	XP_005252031.1:p.Ser1354Ter
XM_005251975.4:c.3788C>A	XP_005252032.1:p.Ser1263Ter
XM_006717096.4:c.5975C>A	XP_006717159.1:p.Ser1992Ter
XM_006717097.4:c.5426C>A	XP_006717160.1:p.Ser1809Ter
XM_006717098.4:c.5153C>A	XP_006717161.1:p.Ser1718Ter
XM_006717101.4:c.4061C>A	XP_006717164.1:p.Ser1354Ter
XM_011518625.3:c.5153C>A	XP_011516927.1:p.Ser1718Ter
XM_011518626.3:c.4883C>A	XP_011516928.1:p.Ser1628Ter
XM_011518628.3:c.4334C>A	XP_011516930.1:p.Ser1445Ter
XM_011518629.3:c.4334C>A	XP_011516931.1:p.Ser1445Ter
XM_017014678.2:c.6248C>A	XP_016870167.1:p.Ser2083Ter
XM_017014679.2:c.5975C>A	XP_016870168.1:p.Ser1992Ter
XM_017014680.2:c.5972C>A	XP_016870169.1:p.Ser1991Ter
XM_017014681.2:c.5156C>A	XP_016870170.1:p.Ser1719Ter
XM_024447530.1:c.6248C>A	XP_024303298.1:p.Ser2083Ter
NM_002160.4:c.5699C>A MANE Select	NP_002151.2:p.Ser1900Ter