Canonical Allele Identifier: CA2785673973
Gene: TNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.115046571_115046572insAGGACACTTCTATCTC , CM000671.2:g.115046571_115046572insAGGACACTTCTATCTC GRCh38
NC_000009.11:g.117808850_117808851insAGGACACTTCTATCTC , CM000671.1:g.117808850_117808851insAGGACACTTCTATCTC GRCh37
NC_000009.10:g.116848671_116848672insAGGACACTTCTATCTC NCBI36
NG_029637.1:g.76692_76693insGAAGTGTCCTGAGATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000476680.2:c.318-4225_318-4224insGAAGTGTCCTGAGATA
ENST00000537320.6:c.3215-4225_3215-4224insGAAGTGTCCTGAGATA ENSP00000443478.1:n.3215-4225_3215-4224insGAAGTGTCCTGAGATA
ENST00000542877.6:c.3880_3881insGAAGTGTCCTGAGATA ENSP00000442242.1:p.Thr1294ArgfsTer11
ENST00000705190.1:c.1912_1913insGAAGTGTCCTGAGATA ENSP00000516083.1:p.Thr638ArgfsTer11
ENST00000705191.1:c.568_569insGAAGTGTCCTGAGATA ENSP00000516084.1:p.Thr190ArgfsTer11
ENST00000705192.1:c.3927_3928insGAAGTGTCCTGAGATA
ENST00000350763.9:c.4969_4970insGAAGTGTCCTGAGATA MANE Select ENSP00000265131.4:p.Thr1657ArgfsTer11
ENST00000341037.8:c.4423_4424insGAAGTGTCCTGAGATA ENSP00000339553.4:p.Thr1475ArgfsTer11
ENST00000350763.8:c.4969_4970insGAAGTGTCCTGAGATA ENSP00000265131.4:p.Thr1657ArgfsTer11
ENST00000423613.6:c.4307-4225_4307-4224insGAAGTGTCCTGAGATA ENSP00000411406.2:n.4307-4225_4307-4224insGAAGTGTCCTGAGATA
ENST00000473855.1:n.287_288insGAAGTGTCCTGAGATA
ENST00000476680.1:n.253-4225_253-4224insGAAGTGTCCTGAGATA
ENST00000498724.5:n.40-4225_40-4224insGAAGTGTCCTGAGATA
ENST00000535648.5:c.3880_3881insGAAGTGTCCTGAGATA ENSP00000438152.2:p.Thr1294ArgfsTer11
ENST00000537320.5:c.3215-4225_3215-4224insGAAGTGTCCTGAGATA ENSP00000443478.1:n.3215-4225_3215-4224insGAAGTGTCCTGAGATA
ENST00000542877.5:c.3880_3881insGAAGTGTCCTGAGATA ENSP00000442242.1:p.Thr1294ArgfsTer11
ENST00000544972.1:c.656_657insGAAGTGTCCTGAGATA
NM_002160.3:c.4969_4970insGAAGTGTCCTGAGATA NP_002151.2:p.Thr1657ArgfsTer11
XM_005251972.2:c.4696_4697insGAAGTGTCCTGAGATA XP_005252029.1:p.Thr1566ArgfsTer11
XM_005251973.2:c.4034-4225_4034-4224insGAAGTGTCCTGAGATA XP_005252030.1:n.4034-4225_4034-4224insGAAGTGTCCTGAGATA
XM_005251974.2:c.3331_3332insGAAGTGTCCTGAGATA XP_005252031.1:p.Thr1111ArgfsTer11
XM_005251975.2:c.3215-4225_3215-4224insGAAGTGTCCTGAGATA XP_005252032.1:n.3215-4225_3215-4224insGAAGTGTCCTGAGATA
XM_006717096.2:c.5245_5246insGAAGTGTCCTGAGATA XP_006717159.1:p.Thr1749ArgfsTer11
XM_006717097.2:c.4696_4697insGAAGTGTCCTGAGATA XP_006717160.1:p.Thr1566ArgfsTer11
XM_006717098.2:c.4423_4424insGAAGTGTCCTGAGATA XP_006717161.1:p.Thr1475ArgfsTer11
XM_006717100.2:c.4307-4225_4307-4224insGAAGTGTCCTGAGATA XP_006717163.1:n.4307-4225_4307-4224insGAAGTGTCCTGAGATA
XM_006717101.2:c.3488-4225_3488-4224insGAAGTGTCCTGAGATA XP_006717164.1:n.3488-4225_3488-4224insGAAGTGTCCTGAGATA
XM_011518622.1:c.4972_4973insGAAGTGTCCTGAGATA XP_011516924.1:p.Thr1658ArgfsTer11
XM_011518623.1:c.4972_4973insGAAGTGTCCTGAGATA XP_011516925.1:p.Thr1658ArgfsTer11
XM_011518624.1:c.4426_4427insGAAGTGTCCTGAGATA XP_011516926.1:p.Thr1476ArgfsTer11
XM_011518625.1:c.4580-4225_4580-4224insGAAGTGTCCTGAGATA XP_011516927.1:n.4580-4225_4580-4224insGAAGTGTCCTGAGATA
XM_011518626.1:c.4153_4154insGAAGTGTCCTGAGATA XP_011516928.1:p.Thr1385ArgfsTer11
XM_011518627.1:c.3880_3881insGAAGTGTCCTGAGATA XP_011516929.1:p.Thr1294ArgfsTer11
XM_011518628.1:c.3761-4225_3761-4224insGAAGTGTCCTGAGATA XP_011516930.1:n.3761-4225_3761-4224insGAAGTGTCCTGAGATA
XM_011518629.1:c.3604_3605insGAAGTGTCCTGAGATA XP_011516931.1:p.Thr1202ArgfsTer11
XM_005251972.4:c.4696_4697insGAAGTGTCCTGAGATA XP_005252029.1:p.Thr1566ArgfsTer11
XM_005251973.4:c.4034-4225_4034-4224insGAAGTGTCCTGAGATA XP_005252030.1:n.4034-4225_4034-4224insGAAGTGTCCTGAGATA
XM_005251974.4:c.3331_3332insGAAGTGTCCTGAGATA XP_005252031.1:p.Thr1111ArgfsTer11
XM_005251975.4:c.3215-4225_3215-4224insGAAGTGTCCTGAGATA XP_005252032.1:n.3215-4225_3215-4224insGAAGTGTCCTGAGATA
XM_006717096.4:c.5245_5246insGAAGTGTCCTGAGATA XP_006717159.1:p.Thr1749ArgfsTer11
XM_006717097.4:c.4696_4697insGAAGTGTCCTGAGATA XP_006717160.1:p.Thr1566ArgfsTer11
XM_006717098.4:c.4423_4424insGAAGTGTCCTGAGATA XP_006717161.1:p.Thr1475ArgfsTer11
XM_006717101.4:c.3488-4225_3488-4224insGAAGTGTCCTGAGATA XP_006717164.1:n.3488-4225_3488-4224insGAAGTGTCCTGAGATA
XM_011518625.3:c.4580-4225_4580-4224insGAAGTGTCCTGAGATA XP_011516927.1:n.4580-4225_4580-4224insGAAGTGTCCTGAGATA
XM_011518626.3:c.4153_4154insGAAGTGTCCTGAGATA XP_011516928.1:p.Thr1385ArgfsTer11
XM_011518628.3:c.3761-4225_3761-4224insGAAGTGTCCTGAGATA XP_011516930.1:n.3761-4225_3761-4224insGAAGTGTCCTGAGATA
XM_011518629.3:c.3604_3605insGAAGTGTCCTGAGATA XP_011516931.1:p.Thr1202ArgfsTer11
XM_017014678.2:c.5518_5519insGAAGTGTCCTGAGATA XP_016870167.1:p.Thr1840ArgfsTer11
XM_017014679.2:c.5245_5246insGAAGTGTCCTGAGATA XP_016870168.1:p.Thr1749ArgfsTer11
XM_017014680.2:c.5242_5243insGAAGTGTCCTGAGATA XP_016870169.1:p.Thr1748ArgfsTer11
XM_017014681.2:c.4426_4427insGAAGTGTCCTGAGATA XP_016870170.1:p.Thr1476ArgfsTer11
XM_024447530.1:c.5518_5519insGAAGTGTCCTGAGATA XP_024303298.1:p.Thr1840ArgfsTer11
NM_002160.4:c.4969_4970insGAAGTGTCCTGAGATA MANE Select NP_002151.2:p.Thr1657ArgfsTer11