Canonical Allele Identifier: CA1874118903
Gene: TNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.115046527C= , CM000671.2:g.115046527C= GRCh38
NC_000009.11:g.117808806C= , CM000671.1:g.117808806C= GRCh37
NC_000009.10:g.116848627C= NCBI36
NG_029637.1:g.76731G=

Transcript Alleles

HGVS Amino-acid change
ENST00000476680.2:c.318-4186G=
ENST00000537320.6:c.3215-4186G= ENSP00000443478.1:n.3215-4186G=
ENST00000542877.6:c.3919G= ENSP00000442242.1:p.Ala1307=
ENST00000705190.1:c.1951G= ENSP00000516083.1:p.Ala651=
ENST00000705191.1:c.607G= ENSP00000516084.1:p.Ala203=
ENST00000705192.1:c.3966G=
ENST00000350763.9:c.5008G= MANE Select ENSP00000265131.4:p.Ala1670=
ENST00000341037.8:c.4462G= ENSP00000339553.4:p.Ala1488=
ENST00000350763.8:c.5008G= ENSP00000265131.4:p.Ala1670=
ENST00000423613.6:c.4307-4186G= ENSP00000411406.2:n.4307-4186G=
ENST00000473855.1:n.326G=
ENST00000476680.1:n.253-4186G=
ENST00000498724.5:n.40-4186G=
ENST00000535648.5:c.3919G= ENSP00000438152.2:p.Ala1307=
ENST00000537320.5:c.3215-4186G= ENSP00000443478.1:n.3215-4186G=
ENST00000542877.5:c.3919G= ENSP00000442242.1:p.Ala1307=
ENST00000544972.1:c.695G=
NM_002160.3:c.5008G= NP_002151.2:p.Ala1670=
XM_005251972.2:c.4735G= XP_005252029.1:p.Ala1579=
XM_005251973.2:c.4034-4186G= XP_005252030.1:n.4034-4186G=
XM_005251974.2:c.3370G= XP_005252031.1:p.Ala1124=
XM_005251975.2:c.3215-4186G= XP_005252032.1:n.3215-4186G=
XM_006717096.2:c.5284G= XP_006717159.1:p.Ala1762=
XM_006717097.2:c.4735G= XP_006717160.1:p.Ala1579=
XM_006717098.2:c.4462G= XP_006717161.1:p.Ala1488=
XM_006717100.2:c.4307-4186G= XP_006717163.1:n.4307-4186G=
XM_006717101.2:c.3488-4186G= XP_006717164.1:n.3488-4186G=
XM_011518622.1:c.5011G= XP_011516924.1:p.Ala1671=
XM_011518623.1:c.5011G= XP_011516925.1:p.Ala1671=
XM_011518624.1:c.4465G= XP_011516926.1:p.Ala1489=
XM_011518625.1:c.4580-4186G= XP_011516927.1:n.4580-4186G=
XM_011518626.1:c.4192G= XP_011516928.1:p.Ala1398=
XM_011518627.1:c.3919G= XP_011516929.1:p.Ala1307=
XM_011518628.1:c.3761-4186G= XP_011516930.1:n.3761-4186G=
XM_011518629.1:c.3643G= XP_011516931.1:p.Ala1215=
XM_005251972.4:c.4735G= XP_005252029.1:p.Ala1579=
XM_005251973.4:c.4034-4186G= XP_005252030.1:n.4034-4186G=
XM_005251974.4:c.3370G= XP_005252031.1:p.Ala1124=
XM_005251975.4:c.3215-4186G= XP_005252032.1:n.3215-4186G=
XM_006717096.4:c.5284G= XP_006717159.1:p.Ala1762=
XM_006717097.4:c.4735G= XP_006717160.1:p.Ala1579=
XM_006717098.4:c.4462G= XP_006717161.1:p.Ala1488=
XM_006717101.4:c.3488-4186G= XP_006717164.1:n.3488-4186G=
XM_011518625.3:c.4580-4186G= XP_011516927.1:n.4580-4186G=
XM_011518626.3:c.4192G= XP_011516928.1:p.Ala1398=
XM_011518628.3:c.3761-4186G= XP_011516930.1:n.3761-4186G=
XM_011518629.3:c.3643G= XP_011516931.1:p.Ala1215=
XM_017014678.2:c.5557G= XP_016870167.1:p.Ala1853=
XM_017014679.2:c.5284G= XP_016870168.1:p.Ala1762=
XM_017014680.2:c.5281G= XP_016870169.1:p.Ala1761=
XM_017014681.2:c.4465G= XP_016870170.1:p.Ala1489=
XM_024447530.1:c.5557G= XP_024303298.1:p.Ala1853=
NM_002160.4:c.5008G= MANE Select NP_002151.2:p.Ala1670=