Canonical Allele Identifier: CA1874113622
Gene: TNC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.115035013_115035014delinsCT , CM000671.2:g.115035013_115035014delinsCT GRCh38
NC_000009.11:g.117797292_117797293delinsCT , CM000671.1:g.117797292_117797293delinsCT GRCh37
NC_000009.10:g.116837113_116837114delinsCT NCBI36
NG_029637.1:g.88244_88245delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000537320.6:c.3876+190_3876+191delinsAG ENSP00000443478.1:n.3876+190_3876+191delinsAG
ENST00000542877.6:c.4698+190_4698+191delinsAG ENSP00000442242.1:n.4698+190_4698+191delinsAG
ENST00000705190.1:c.2730+190_2730+191delinsAG ENSP00000516083.1:n.2730+190_2730+191delinsAG
ENST00000705191.1:c.1386+190_1386+191delinsAG ENSP00000516084.1:n.1386+190_1386+191delinsAG
ENST00000705192.1:c.4745+190_4745+191delinsAG
ENST00000350763.9:c.5787+190_5787+191delinsAG MANE Select ENSP00000265131.4:n.5787+190_5787+191delinsAG
ENST00000341037.8:c.5241+190_5241+191delinsAG ENSP00000339553.4:n.5241+190_5241+191delinsAG
ENST00000350763.8:c.5787+190_5787+191delinsAG ENSP00000265131.4:n.5787+190_5787+191delinsAG
ENST00000423613.6:c.4968+190_4968+191delinsAG ENSP00000411406.2:n.4968+190_4968+191delinsAG
ENST00000460345.1:n.369+190_369+191delinsAG
ENST00000535648.5:c.4698+190_4698+191delinsAG ENSP00000438152.2:n.4698+190_4698+191delinsAG
ENST00000537320.5:c.3876+190_3876+191delinsAG ENSP00000443478.1:n.3876+190_3876+191delinsAG
ENST00000542877.5:c.4698+190_4698+191delinsAG ENSP00000442242.1:n.4698+190_4698+191delinsAG
ENST00000544972.1:c.1474+190_1474+191delinsAG
NM_002160.3:c.5787+190_5787+191delinsAG NP_002151.2:n.5787+190_5787+191delinsAG
XM_005251972.2:c.5514+190_5514+191delinsAG XP_005252029.1:n.5514+190_5514+191delinsAG
XM_005251973.2:c.4695+190_4695+191delinsAG XP_005252030.1:n.4695+190_4695+191delinsAG
XM_005251974.2:c.4149+190_4149+191delinsAG XP_005252031.1:n.4149+190_4149+191delinsAG
XM_005251975.2:c.3876+190_3876+191delinsAG XP_005252032.1:n.3876+190_3876+191delinsAG
XM_006717096.2:c.6063+190_6063+191delinsAG XP_006717159.1:n.6063+190_6063+191delinsAG
XM_006717097.2:c.5514+190_5514+191delinsAG XP_006717160.1:n.5514+190_5514+191delinsAG
XM_006717098.2:c.5241+190_5241+191delinsAG XP_006717161.1:n.5241+190_5241+191delinsAG
XM_006717100.2:c.4968+190_4968+191delinsAG XP_006717163.1:n.4968+190_4968+191delinsAG
XM_006717101.2:c.4149+190_4149+191delinsAG XP_006717164.1:n.4149+190_4149+191delinsAG
XM_011518622.1:c.5790+190_5790+191delinsAG XP_011516924.1:n.5790+190_5790+191delinsAG
XM_011518623.1:c.5790+190_5790+191delinsAG XP_011516925.1:n.5790+190_5790+191delinsAG
XM_011518624.1:c.5244+190_5244+191delinsAG XP_011516926.1:n.5244+190_5244+191delinsAG
XM_011518625.1:c.5241+190_5241+191delinsAG XP_011516927.1:n.5241+190_5241+191delinsAG
XM_011518626.1:c.4971+190_4971+191delinsAG XP_011516928.1:n.4971+190_4971+191delinsAG
XM_011518627.1:c.4698+190_4698+191delinsAG XP_011516929.1:n.4698+190_4698+191delinsAG
XM_011518628.1:c.4422+190_4422+191delinsAG XP_011516930.1:n.4422+190_4422+191delinsAG
XM_011518629.1:c.4422+190_4422+191delinsAG XP_011516931.1:n.4422+190_4422+191delinsAG
XM_005251972.4:c.5514+190_5514+191delinsAG XP_005252029.1:n.5514+190_5514+191delinsAG
XM_005251973.4:c.4695+190_4695+191delinsAG XP_005252030.1:n.4695+190_4695+191delinsAG
XM_005251974.4:c.4149+190_4149+191delinsAG XP_005252031.1:n.4149+190_4149+191delinsAG
XM_005251975.4:c.3876+190_3876+191delinsAG XP_005252032.1:n.3876+190_3876+191delinsAG
XM_006717096.4:c.6063+190_6063+191delinsAG XP_006717159.1:n.6063+190_6063+191delinsAG
XM_006717097.4:c.5514+190_5514+191delinsAG XP_006717160.1:n.5514+190_5514+191delinsAG
XM_006717098.4:c.5241+190_5241+191delinsAG XP_006717161.1:n.5241+190_5241+191delinsAG
XM_006717101.4:c.4149+190_4149+191delinsAG XP_006717164.1:n.4149+190_4149+191delinsAG
XM_011518625.3:c.5241+190_5241+191delinsAG XP_011516927.1:n.5241+190_5241+191delinsAG
XM_011518626.3:c.4971+190_4971+191delinsAG XP_011516928.1:n.4971+190_4971+191delinsAG
XM_011518628.3:c.4422+190_4422+191delinsAG XP_011516930.1:n.4422+190_4422+191delinsAG
XM_011518629.3:c.4422+190_4422+191delinsAG XP_011516931.1:n.4422+190_4422+191delinsAG
XM_017014678.2:c.6336+190_6336+191delinsAG XP_016870167.1:n.6336+190_6336+191delinsAG
XM_017014679.2:c.6063+190_6063+191delinsAG XP_016870168.1:n.6063+190_6063+191delinsAG
XM_017014680.2:c.6060+190_6060+191delinsAG XP_016870169.1:n.6060+190_6060+191delinsAG
XM_017014681.2:c.5244+190_5244+191delinsAG XP_016870170.1:n.5244+190_5244+191delinsAG
XM_024447530.1:c.6336+190_6336+191delinsAG XP_024303298.1:n.6336+190_6336+191delinsAG
NM_002160.4:c.5787+190_5787+191delinsAG MANE Select NP_002151.2:n.5787+190_5787+191delinsAG
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