Canonical Allele Identifier: CA1874118704
Gene: TNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.115046066G= , CM000671.2:g.115046066G= GRCh38
NC_000009.11:g.117808345G= , CM000671.1:g.117808345G= GRCh37
NC_000009.10:g.116848166G= NCBI36
NG_029637.1:g.77192C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000476680.2:c.318-3725C=
ENST00000537320.6:c.3215-3725C= ENSP00000443478.1:n.3215-3725C=
ENST00000542877.6:c.4036+344C= ENSP00000442242.1:n.4036+344C=
ENST00000705190.1:c.2068+344C= ENSP00000516083.1:n.2068+344C=
ENST00000705191.1:c.724+344C= ENSP00000516084.1:n.724+344C=
ENST00000705192.1:c.4083+344C=
ENST00000350763.9:c.5125+344C= MANE Select ENSP00000265131.4:n.5125+344C=
ENST00000341037.8:c.4579+344C= ENSP00000339553.4:n.4579+344C=
ENST00000350763.8:c.5125+344C= ENSP00000265131.4:n.5125+344C=
ENST00000423613.6:c.4307-3725C= ENSP00000411406.2:n.4307-3725C=
ENST00000476680.1:n.253-3725C=
ENST00000498724.5:n.40-3725C=
ENST00000535648.5:c.4036+344C= ENSP00000438152.2:n.4036+344C=
ENST00000537320.5:c.3215-3725C= ENSP00000443478.1:n.3215-3725C=
ENST00000542877.5:c.4036+344C= ENSP00000442242.1:n.4036+344C=
ENST00000544972.1:c.812+344C=
NM_002160.3:c.5125+344C= NP_002151.2:n.5125+344C=
XM_005251972.2:c.4852+344C= XP_005252029.1:n.4852+344C=
XM_005251973.2:c.4034-3725C= XP_005252030.1:n.4034-3725C=
XM_005251974.2:c.3487+344C= XP_005252031.1:n.3487+344C=
XM_005251975.2:c.3215-3725C= XP_005252032.1:n.3215-3725C=
XM_006717096.2:c.5401+344C= XP_006717159.1:n.5401+344C=
XM_006717097.2:c.4852+344C= XP_006717160.1:n.4852+344C=
XM_006717098.2:c.4579+344C= XP_006717161.1:n.4579+344C=
XM_006717100.2:c.4307-3725C= XP_006717163.1:n.4307-3725C=
XM_006717101.2:c.3488-3725C= XP_006717164.1:n.3488-3725C=
XM_011518622.1:c.5128+344C= XP_011516924.1:n.5128+344C=
XM_011518623.1:c.5128+344C= XP_011516925.1:n.5128+344C=
XM_011518624.1:c.4582+344C= XP_011516926.1:n.4582+344C=
XM_011518625.1:c.4580-3725C= XP_011516927.1:n.4580-3725C=
XM_011518626.1:c.4309+344C= XP_011516928.1:n.4309+344C=
XM_011518627.1:c.4036+344C= XP_011516929.1:n.4036+344C=
XM_011518628.1:c.3761-3725C= XP_011516930.1:n.3761-3725C=
XM_011518629.1:c.3760+344C= XP_011516931.1:n.3760+344C=
XM_005251972.4:c.4852+344C= XP_005252029.1:n.4852+344C=
XM_005251973.4:c.4034-3725C= XP_005252030.1:n.4034-3725C=
XM_005251974.4:c.3487+344C= XP_005252031.1:n.3487+344C=
XM_005251975.4:c.3215-3725C= XP_005252032.1:n.3215-3725C=
XM_006717096.4:c.5401+344C= XP_006717159.1:n.5401+344C=
XM_006717097.4:c.4852+344C= XP_006717160.1:n.4852+344C=
XM_006717098.4:c.4579+344C= XP_006717161.1:n.4579+344C=
XM_006717101.4:c.3488-3725C= XP_006717164.1:n.3488-3725C=
XM_011518625.3:c.4580-3725C= XP_011516927.1:n.4580-3725C=
XM_011518626.3:c.4309+344C= XP_011516928.1:n.4309+344C=
XM_011518628.3:c.3761-3725C= XP_011516930.1:n.3761-3725C=
XM_011518629.3:c.3760+344C= XP_011516931.1:n.3760+344C=
XM_017014678.2:c.5674+344C= XP_016870167.1:n.5674+344C=
XM_017014679.2:c.5401+344C= XP_016870168.1:n.5401+344C=
XM_017014680.2:c.5398+344C= XP_016870169.1:n.5398+344C=
XM_017014681.2:c.4582+344C= XP_016870170.1:n.4582+344C=
XM_024447530.1:c.5674+344C= XP_024303298.1:n.5674+344C=
NM_002160.4:c.5125+344C= MANE Select NP_002151.2:n.5125+344C=