Canonical Allele Identifier: CA1874112806
Gene: TNC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.115033221_115033222delinsAT , CM000671.2:g.115033221_115033222delinsAT GRCh38
NC_000009.11:g.117795500_117795501delinsAT , CM000671.1:g.117795500_117795501delinsAT GRCh37
NC_000009.10:g.116835321_116835322delinsAT NCBI36
NG_029637.1:g.90036_90037delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000537320.6:c.3877-1537_3877-1536delinsAT ENSP00000443478.1:n.3877-1537_3877-1536delinsAT
ENST00000542877.6:c.4699-1537_4699-1536delinsAT ENSP00000442242.1:n.4699-1537_4699-1536delinsAT
ENST00000705190.1:c.2731-1537_2731-1536delinsAT ENSP00000516083.1:n.2731-1537_2731-1536delinsAT
ENST00000705191.1:c.1387-1537_1387-1536delinsAT ENSP00000516084.1:n.1387-1537_1387-1536delinsAT
ENST00000705192.1:c.4746-1537_4746-1536delinsAT
ENST00000350763.9:c.5788-1537_5788-1536delinsAT MANE Select ENSP00000265131.4:n.5788-1537_5788-1536delinsAT
ENST00000341037.8:c.5242-1537_5242-1536delinsAT ENSP00000339553.4:n.5242-1537_5242-1536delinsAT
ENST00000350763.8:c.5788-1537_5788-1536delinsAT ENSP00000265131.4:n.5788-1537_5788-1536delinsAT
ENST00000423613.6:c.4969-1537_4969-1536delinsAT ENSP00000411406.2:n.4969-1537_4969-1536delinsAT
ENST00000460345.1:n.370-1537_370-1536delinsAT
ENST00000535648.5:c.4699-1537_4699-1536delinsAT ENSP00000438152.2:n.4699-1537_4699-1536delinsAT
ENST00000537320.5:c.3877-1537_3877-1536delinsAT ENSP00000443478.1:n.3877-1537_3877-1536delinsAT
ENST00000542877.5:c.4699-1537_4699-1536delinsAT ENSP00000442242.1:n.4699-1537_4699-1536delinsAT
ENST00000544972.1:c.1475-1537_1475-1536delinsAT
NM_002160.3:c.5788-1537_5788-1536delinsAT NP_002151.2:n.5788-1537_5788-1536delinsAT
XM_005251972.2:c.5515-1537_5515-1536delinsAT XP_005252029.1:n.5515-1537_5515-1536delinsAT
XM_005251973.2:c.4696-1537_4696-1536delinsAT XP_005252030.1:n.4696-1537_4696-1536delinsAT
XM_005251974.2:c.4150-1537_4150-1536delinsAT XP_005252031.1:n.4150-1537_4150-1536delinsAT
XM_005251975.2:c.3877-1537_3877-1536delinsAT XP_005252032.1:n.3877-1537_3877-1536delinsAT
XM_006717096.2:c.6064-1537_6064-1536delinsAT XP_006717159.1:n.6064-1537_6064-1536delinsAT
XM_006717097.2:c.5515-1537_5515-1536delinsAT XP_006717160.1:n.5515-1537_5515-1536delinsAT
XM_006717098.2:c.5242-1537_5242-1536delinsAT XP_006717161.1:n.5242-1537_5242-1536delinsAT
XM_006717100.2:c.4969-1537_4969-1536delinsAT XP_006717163.1:n.4969-1537_4969-1536delinsAT
XM_006717101.2:c.4150-1537_4150-1536delinsAT XP_006717164.1:n.4150-1537_4150-1536delinsAT
XM_011518622.1:c.5791-1537_5791-1536delinsAT XP_011516924.1:n.5791-1537_5791-1536delinsAT
XM_011518623.1:c.5791-1537_5791-1536delinsAT XP_011516925.1:n.5791-1537_5791-1536delinsAT
XM_011518624.1:c.5245-1537_5245-1536delinsAT XP_011516926.1:n.5245-1537_5245-1536delinsAT
XM_011518625.1:c.5242-1537_5242-1536delinsAT XP_011516927.1:n.5242-1537_5242-1536delinsAT
XM_011518626.1:c.4972-1537_4972-1536delinsAT XP_011516928.1:n.4972-1537_4972-1536delinsAT
XM_011518627.1:c.4699-1537_4699-1536delinsAT XP_011516929.1:n.4699-1537_4699-1536delinsAT
XM_011518628.1:c.4423-1537_4423-1536delinsAT XP_011516930.1:n.4423-1537_4423-1536delinsAT
XM_011518629.1:c.4423-1537_4423-1536delinsAT XP_011516931.1:n.4423-1537_4423-1536delinsAT
XM_005251972.4:c.5515-1537_5515-1536delinsAT XP_005252029.1:n.5515-1537_5515-1536delinsAT
XM_005251973.4:c.4696-1537_4696-1536delinsAT XP_005252030.1:n.4696-1537_4696-1536delinsAT
XM_005251974.4:c.4150-1537_4150-1536delinsAT XP_005252031.1:n.4150-1537_4150-1536delinsAT
XM_005251975.4:c.3877-1537_3877-1536delinsAT XP_005252032.1:n.3877-1537_3877-1536delinsAT
XM_006717096.4:c.6064-1537_6064-1536delinsAT XP_006717159.1:n.6064-1537_6064-1536delinsAT
XM_006717097.4:c.5515-1537_5515-1536delinsAT XP_006717160.1:n.5515-1537_5515-1536delinsAT
XM_006717098.4:c.5242-1537_5242-1536delinsAT XP_006717161.1:n.5242-1537_5242-1536delinsAT
XM_006717101.4:c.4150-1537_4150-1536delinsAT XP_006717164.1:n.4150-1537_4150-1536delinsAT
XM_011518625.3:c.5242-1537_5242-1536delinsAT XP_011516927.1:n.5242-1537_5242-1536delinsAT
XM_011518626.3:c.4972-1537_4972-1536delinsAT XP_011516928.1:n.4972-1537_4972-1536delinsAT
XM_011518628.3:c.4423-1537_4423-1536delinsAT XP_011516930.1:n.4423-1537_4423-1536delinsAT
XM_011518629.3:c.4423-1537_4423-1536delinsAT XP_011516931.1:n.4423-1537_4423-1536delinsAT
XM_017014678.2:c.6337-1537_6337-1536delinsAT XP_016870167.1:n.6337-1537_6337-1536delinsAT
XM_017014679.2:c.6064-1537_6064-1536delinsAT XP_016870168.1:n.6064-1537_6064-1536delinsAT
XM_017014680.2:c.6061-1537_6061-1536delinsAT XP_016870169.1:n.6061-1537_6061-1536delinsAT
XM_017014681.2:c.5245-1537_5245-1536delinsAT XP_016870170.1:n.5245-1537_5245-1536delinsAT
XM_024447530.1:c.6337-1537_6337-1536delinsAT XP_024303298.1:n.6337-1537_6337-1536delinsAT
NM_002160.4:c.5788-1537_5788-1536delinsAT MANE Select NP_002151.2:n.5788-1537_5788-1536delinsAT
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