Canonical Allele Identifier: CA918540850
Gene: TNC HGNC NCBI

Linked Data

dbSNP Id: rs1564433410

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.115046594del , CM000671.2:g.115046594del GRCh38
NC_000009.11:g.117808873del , CM000671.1:g.117808873del GRCh37
NC_000009.10:g.116848694del NCBI36
NG_029637.1:g.76664del

Transcript Alleles

HGVS Amino-acid Change
ENST00000476680.2:c.318-4253del
ENST00000537320.6:c.3215-4253del ENSP00000443478.1:n.3215-4253del
ENST00000542877.6:c.3852del ENSP00000442242.1:p.Phe1284LeufsTer20
ENST00000705190.1:c.1884del ENSP00000516083.1:p.Phe628LeufsTer20
ENST00000705191.1:c.540del ENSP00000516084.1:p.Phe180LeufsTer20
ENST00000705192.1:c.3899del
ENST00000350763.9:c.4941del MANE Select ENSP00000265131.4:p.Phe1647LeufsTer20
ENST00000341037.8:c.4395del ENSP00000339553.4:p.Phe1465LeufsTer20
ENST00000350763.8:c.4941del ENSP00000265131.4:p.Phe1647LeufsTer20
ENST00000423613.6:c.4307-4253del ENSP00000411406.2:n.4307-4253del
ENST00000473855.1:n.259del
ENST00000476680.1:n.253-4253del
ENST00000498724.5:n.40-4253del
ENST00000535648.5:c.3852del ENSP00000438152.2:p.Phe1284LeufsTer20
ENST00000537320.5:c.3215-4253del ENSP00000443478.1:n.3215-4253del
ENST00000542877.5:c.3852del ENSP00000442242.1:p.Phe1284LeufsTer20
ENST00000544972.1:c.628del
NM_002160.3:c.4941del NP_002151.2:p.Phe1647LeufsTer20
XM_005251972.2:c.4668del XP_005252029.1:p.Phe1556LeufsTer20
XM_005251973.2:c.4034-4253del XP_005252030.1:n.4034-4253del
XM_005251974.2:c.3303del XP_005252031.1:p.Phe1101LeufsTer20
XM_005251975.2:c.3215-4253del XP_005252032.1:n.3215-4253del
XM_006717096.2:c.5217del XP_006717159.1:p.Phe1739LeufsTer20
XM_006717097.2:c.4668del XP_006717160.1:p.Phe1556LeufsTer20
XM_006717098.2:c.4395del XP_006717161.1:p.Phe1465LeufsTer20
XM_006717100.2:c.4307-4253del XP_006717163.1:n.4307-4253del
XM_006717101.2:c.3488-4253del XP_006717164.1:n.3488-4253del
XM_011518622.1:c.4944del XP_011516924.1:p.Phe1648LeufsTer20
XM_011518623.1:c.4944del XP_011516925.1:p.Phe1648LeufsTer20
XM_011518624.1:c.4398del XP_011516926.1:p.Phe1466LeufsTer20
XM_011518625.1:c.4580-4253del XP_011516927.1:n.4580-4253del
XM_011518626.1:c.4125del XP_011516928.1:p.Phe1375LeufsTer20
XM_011518627.1:c.3852del XP_011516929.1:p.Phe1284LeufsTer20
XM_011518628.1:c.3761-4253del XP_011516930.1:n.3761-4253del
XM_011518629.1:c.3576del XP_011516931.1:p.Phe1192LeufsTer20
XM_005251972.4:c.4668del XP_005252029.1:p.Phe1556LeufsTer20
XM_005251973.4:c.4034-4253del XP_005252030.1:n.4034-4253del
XM_005251974.4:c.3303del XP_005252031.1:p.Phe1101LeufsTer20
XM_005251975.4:c.3215-4253del XP_005252032.1:n.3215-4253del
XM_006717096.4:c.5217del XP_006717159.1:p.Phe1739LeufsTer20
XM_006717097.4:c.4668del XP_006717160.1:p.Phe1556LeufsTer20
XM_006717098.4:c.4395del XP_006717161.1:p.Phe1465LeufsTer20
XM_006717101.4:c.3488-4253del XP_006717164.1:n.3488-4253del
XM_011518625.3:c.4580-4253del XP_011516927.1:n.4580-4253del
XM_011518626.3:c.4125del XP_011516928.1:p.Phe1375LeufsTer20
XM_011518628.3:c.3761-4253del XP_011516930.1:n.3761-4253del
XM_011518629.3:c.3576del XP_011516931.1:p.Phe1192LeufsTer20
XM_017014678.2:c.5490del XP_016870167.1:p.Phe1830LeufsTer20
XM_017014679.2:c.5217del XP_016870168.1:p.Phe1739LeufsTer20
XM_017014680.2:c.5214del XP_016870169.1:p.Phe1738LeufsTer20
XM_017014681.2:c.4398del XP_016870170.1:p.Phe1466LeufsTer20
XM_024447530.1:c.5490del XP_024303298.1:p.Phe1830LeufsTer20
NM_002160.4:c.4941del MANE Select NP_002151.2:p.Phe1647LeufsTer20