Canonical Allele Identifier: CA1874116339
Gene: TNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.115041016C= , CM000671.2:g.115041016C= GRCh38
NC_000009.11:g.117803295C= , CM000671.1:g.117803295C= GRCh37
NC_000009.10:g.116843116C= NCBI36
NG_029637.1:g.82242G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000476680.2:c.509G=
ENST00000537320.6:c.3406G= ENSP00000443478.1:p.Val1136=
ENST00000542877.6:c.4228G= ENSP00000442242.1:p.Val1410=
ENST00000705190.1:c.2260G= ENSP00000516083.1:p.Val754=
ENST00000705191.1:c.916G= ENSP00000516084.1:p.Val306=
ENST00000705192.1:c.4275G=
ENST00000350763.9:c.5317G= MANE Select ENSP00000265131.4:p.Val1773=
ENST00000341037.8:c.4771G= ENSP00000339553.4:p.Val1591=
ENST00000350763.8:c.5317G= ENSP00000265131.4:p.Val1773=
ENST00000423613.6:c.4498G= ENSP00000411406.2:p.Val1500=
ENST00000476680.1:n.444G=
ENST00000498724.5:n.231G=
ENST00000535648.5:c.4228G= ENSP00000438152.2:p.Val1410=
ENST00000537320.5:c.3406G= ENSP00000443478.1:p.Val1136=
ENST00000542877.5:c.4228G= ENSP00000442242.1:p.Val1410=
ENST00000544972.1:c.1004G=
NM_002160.3:c.5317G= NP_002151.2:p.Val1773=
XM_005251972.2:c.5044G= XP_005252029.1:p.Val1682=
XM_005251973.2:c.4225G= XP_005252030.1:p.Val1409=
XM_005251974.2:c.3679G= XP_005252031.1:p.Val1227=
XM_005251975.2:c.3406G= XP_005252032.1:p.Val1136=
XM_006717096.2:c.5593G= XP_006717159.1:p.Val1865=
XM_006717097.2:c.5044G= XP_006717160.1:p.Val1682=
XM_006717098.2:c.4771G= XP_006717161.1:p.Val1591=
XM_006717100.2:c.4498G= XP_006717163.1:p.Val1500=
XM_006717101.2:c.3679G= XP_006717164.1:p.Val1227=
XM_011518622.1:c.5320G= XP_011516924.1:p.Val1774=
XM_011518623.1:c.5320G= XP_011516925.1:p.Val1774=
XM_011518624.1:c.4774G= XP_011516926.1:p.Val1592=
XM_011518625.1:c.4771G= XP_011516927.1:p.Val1591=
XM_011518626.1:c.4501G= XP_011516928.1:p.Val1501=
XM_011518627.1:c.4228G= XP_011516929.1:p.Val1410=
XM_011518628.1:c.3952G= XP_011516930.1:p.Val1318=
XM_011518629.1:c.3952G= XP_011516931.1:p.Val1318=
XM_005251972.4:c.5044G= XP_005252029.1:p.Val1682=
XM_005251973.4:c.4225G= XP_005252030.1:p.Val1409=
XM_005251974.4:c.3679G= XP_005252031.1:p.Val1227=
XM_005251975.4:c.3406G= XP_005252032.1:p.Val1136=
XM_006717096.4:c.5593G= XP_006717159.1:p.Val1865=
XM_006717097.4:c.5044G= XP_006717160.1:p.Val1682=
XM_006717098.4:c.4771G= XP_006717161.1:p.Val1591=
XM_006717101.4:c.3679G= XP_006717164.1:p.Val1227=
XM_011518625.3:c.4771G= XP_011516927.1:p.Val1591=
XM_011518626.3:c.4501G= XP_011516928.1:p.Val1501=
XM_011518628.3:c.3952G= XP_011516930.1:p.Val1318=
XM_011518629.3:c.3952G= XP_011516931.1:p.Val1318=
XM_017014678.2:c.5866G= XP_016870167.1:p.Val1956=
XM_017014679.2:c.5593G= XP_016870168.1:p.Val1865=
XM_017014680.2:c.5590G= XP_016870169.1:p.Val1864=
XM_017014681.2:c.4774G= XP_016870170.1:p.Val1592=
XM_024447530.1:c.5866G= XP_024303298.1:p.Val1956=
NM_002160.4:c.5317G= MANE Select NP_002151.2:p.Val1773=