Canonical Allele Identifier: CA5207617
Community Standard Title: NM_002160.4(TNC):c.5531C>T (p.Thr1844Met)
Gene: TNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.115036223G>A , CM000671.2:g.115036223G>A GRCh38
NC_000009.11:g.117798502G>A , CM000671.1:g.117798502G>A GRCh37
NC_000009.10:g.116838323G>A NCBI36
NG_029637.1:g.87035C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002160.4:c.5531C>T MANE Select NP_002151.2:p.Thr1844Met
ENST00000350763.9:c.5531C>T MANE Select ENSP00000265131.4:p.Thr1844Met
NM_002160.3:c.5531C>T NP_002151.2:p.Thr1844Met
ENST00000341037.8:c.4985C>T ENSP00000339553.4:p.Thr1662Met
ENST00000350763.8:c.5531C>T ENSP00000265131.4:p.Thr1844Met
ENST00000423613.6:c.4712C>T ENSP00000411406.2:p.Thr1571Met
ENST00000476680.1:n.658C>T
ENST00000476680.2:c.723C>T
ENST00000498724.5:n.445C>T
ENST00000535648.5:c.4442C>T ENSP00000438152.2:p.Thr1481Met
ENST00000537320.5:c.3620C>T ENSP00000443478.1:p.Thr1207Met
ENST00000537320.6:c.3620C>T ENSP00000443478.1:p.Thr1207Met
ENST00000542877.5:c.4442C>T ENSP00000442242.1:p.Thr1481Met
ENST00000542877.6:c.4442C>T ENSP00000442242.1:p.Thr1481Met
ENST00000544972.1:c.1218C>T
ENST00000705190.1:c.2474C>T ENSP00000516083.1:p.Thr825Met
ENST00000705191.1:c.1130C>T ENSP00000516084.1:p.Thr377Met
ENST00000705192.1:c.4489C>T
XM_005251972.2:c.5258C>T XP_005252029.1:p.Thr1753Met
XM_005251972.4:c.5258C>T XP_005252029.1:p.Thr1753Met
XM_005251973.2:c.4439C>T XP_005252030.1:p.Thr1480Met
XM_005251973.4:c.4439C>T XP_005252030.1:p.Thr1480Met
XM_005251974.2:c.3893C>T XP_005252031.1:p.Thr1298Met
XM_005251974.4:c.3893C>T XP_005252031.1:p.Thr1298Met
XM_005251975.2:c.3620C>T XP_005252032.1:p.Thr1207Met
XM_005251975.4:c.3620C>T XP_005252032.1:p.Thr1207Met
XM_006717096.2:c.5807C>T XP_006717159.1:p.Thr1936Met
XM_006717096.4:c.5807C>T XP_006717159.1:p.Thr1936Met
XM_006717097.2:c.5258C>T XP_006717160.1:p.Thr1753Met
XM_006717097.4:c.5258C>T XP_006717160.1:p.Thr1753Met
XM_006717098.2:c.4985C>T XP_006717161.1:p.Thr1662Met
XM_006717098.4:c.4985C>T XP_006717161.1:p.Thr1662Met
XM_006717100.2:c.4712C>T XP_006717163.1:p.Thr1571Met
XM_006717101.2:c.3893C>T XP_006717164.1:p.Thr1298Met
XM_006717101.4:c.3893C>T XP_006717164.1:p.Thr1298Met
XM_011518622.1:c.5534C>T XP_011516924.1:p.Thr1845Met
XM_011518623.1:c.5534C>T XP_011516925.1:p.Thr1845Met
XM_011518624.1:c.4988C>T XP_011516926.1:p.Thr1663Met
XM_011518625.1:c.4985C>T XP_011516927.1:p.Thr1662Met
XM_011518625.3:c.4985C>T XP_011516927.1:p.Thr1662Met
XM_011518626.1:c.4715C>T XP_011516928.1:p.Thr1572Met
XM_011518626.3:c.4715C>T XP_011516928.1:p.Thr1572Met
XM_011518627.1:c.4442C>T XP_011516929.1:p.Thr1481Met
XM_011518628.1:c.4166C>T XP_011516930.1:p.Thr1389Met
XM_011518628.3:c.4166C>T XP_011516930.1:p.Thr1389Met
XM_011518629.1:c.4166C>T XP_011516931.1:p.Thr1389Met
XM_011518629.3:c.4166C>T XP_011516931.1:p.Thr1389Met
XM_017014678.2:c.6080C>T XP_016870167.1:p.Thr2027Met
XM_017014679.2:c.5807C>T XP_016870168.1:p.Thr1936Met
XM_017014680.2:c.5804C>T XP_016870169.1:p.Thr1935Met
XM_017014681.2:c.4988C>T XP_016870170.1:p.Thr1663Met
XM_024447530.1:c.6080C>T XP_024303298.1:p.Thr2027Met