Canonical Allele Identifier: CA5207727
Gene: TNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.115042265T>C , CM000671.2:g.115042265T>C GRCh38
NC_000009.11:g.117804544T>C , CM000671.1:g.117804544T>C GRCh37
NC_000009.10:g.116844365T>C NCBI36
NG_029637.1:g.80993A>G

Transcript Alleles

HGVS Amino-acid Change
NM_002160.4:c.5202A>G MANE Select NP_002151.2:p.Thr1734=
ENST00000350763.9:c.5202A>G MANE Select ENSP00000265131.4:p.Thr1734=
NM_002160.3:c.5202A>G NP_002151.2:p.Thr1734=
ENST00000341037.8:c.4656A>G ENSP00000339553.4:p.Thr1552=
ENST00000350763.8:c.5202A>G ENSP00000265131.4:p.Thr1734=
ENST00000423613.6:c.4383A>G ENSP00000411406.2:p.Thr1461=
ENST00000476680.1:n.329A>G
ENST00000476680.2:c.394A>G
ENST00000498724.5:n.116A>G
ENST00000535648.5:c.4113A>G ENSP00000438152.2:p.Thr1371=
ENST00000537320.5:c.3291A>G ENSP00000443478.1:p.Thr1097=
ENST00000537320.6:c.3291A>G ENSP00000443478.1:p.Thr1097=
ENST00000542877.5:c.4113A>G ENSP00000442242.1:p.Thr1371=
ENST00000542877.6:c.4113A>G ENSP00000442242.1:p.Thr1371=
ENST00000544972.1:c.889A>G
ENST00000705190.1:c.2145A>G ENSP00000516083.1:p.Thr715=
ENST00000705191.1:c.801A>G ENSP00000516084.1:p.Thr267=
ENST00000705192.1:c.4160A>G
XM_005251972.2:c.4929A>G XP_005252029.1:p.Thr1643=
XM_005251972.4:c.4929A>G XP_005252029.1:p.Thr1643=
XM_005251973.2:c.4110A>G XP_005252030.1:p.Thr1370=
XM_005251973.4:c.4110A>G XP_005252030.1:p.Thr1370=
XM_005251974.2:c.3564A>G XP_005252031.1:p.Thr1188=
XM_005251974.4:c.3564A>G XP_005252031.1:p.Thr1188=
XM_005251975.2:c.3291A>G XP_005252032.1:p.Thr1097=
XM_005251975.4:c.3291A>G XP_005252032.1:p.Thr1097=
XM_006717096.2:c.5478A>G XP_006717159.1:p.Thr1826=
XM_006717096.4:c.5478A>G XP_006717159.1:p.Thr1826=
XM_006717097.2:c.4929A>G XP_006717160.1:p.Thr1643=
XM_006717097.4:c.4929A>G XP_006717160.1:p.Thr1643=
XM_006717098.2:c.4656A>G XP_006717161.1:p.Thr1552=
XM_006717098.4:c.4656A>G XP_006717161.1:p.Thr1552=
XM_006717100.2:c.4383A>G XP_006717163.1:p.Thr1461=
XM_006717101.2:c.3564A>G XP_006717164.1:p.Thr1188=
XM_006717101.4:c.3564A>G XP_006717164.1:p.Thr1188=
XM_011518622.1:c.5205A>G XP_011516924.1:p.Thr1735=
XM_011518623.1:c.5205A>G XP_011516925.1:p.Thr1735=
XM_011518624.1:c.4659A>G XP_011516926.1:p.Thr1553=
XM_011518625.1:c.4656A>G XP_011516927.1:p.Thr1552=
XM_011518625.3:c.4656A>G XP_011516927.1:p.Thr1552=
XM_011518626.1:c.4386A>G XP_011516928.1:p.Thr1462=
XM_011518626.3:c.4386A>G XP_011516928.1:p.Thr1462=
XM_011518627.1:c.4113A>G XP_011516929.1:p.Thr1371=
XM_011518628.1:c.3837A>G XP_011516930.1:p.Thr1279=
XM_011518628.3:c.3837A>G XP_011516930.1:p.Thr1279=
XM_011518629.1:c.3837A>G XP_011516931.1:p.Thr1279=
XM_011518629.3:c.3837A>G XP_011516931.1:p.Thr1279=
XM_017014678.2:c.5751A>G XP_016870167.1:p.Thr1917=
XM_017014679.2:c.5478A>G XP_016870168.1:p.Thr1826=
XM_017014680.2:c.5475A>G XP_016870169.1:p.Thr1825=
XM_017014681.2:c.4659A>G XP_016870170.1:p.Thr1553=
XM_024447530.1:c.5751A>G XP_024303298.1:p.Thr1917=