Canonical Allele Identifier: CA1874118708

Gene: TNC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115046070_115046071delinsGT , CM000671.2:g.115046070_115046071delinsGT	GRCh38
NC_000009.11:g.117808349_117808350delinsGT , CM000671.1:g.117808349_117808350delinsGT	GRCh37
NC_000009.10:g.116848170_116848171delinsGT	NCBI36
NG_029637.1:g.77187_77188delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476680.2:c.318-3730_318-3729delinsAC
ENST00000537320.6:c.3215-3730_3215-3729delinsAC	ENSP00000443478.1:n.3215-3730_3215-3729delinsAC
ENST00000542877.6:c.4036+339_4036+340delinsAC	ENSP00000442242.1:n.4036+339_4036+340delinsAC
ENST00000705190.1:c.2068+339_2068+340delinsAC	ENSP00000516083.1:n.2068+339_2068+340delinsAC
ENST00000705191.1:c.724+339_724+340delinsAC	ENSP00000516084.1:n.724+339_724+340delinsAC
ENST00000705192.1:c.4083+339_4083+340delinsAC
ENST00000350763.9:c.5125+339_5125+340delinsAC MANE Select	ENSP00000265131.4:n.5125+339_5125+340delinsAC
ENST00000341037.8:c.4579+339_4579+340delinsAC	ENSP00000339553.4:n.4579+339_4579+340delinsAC
ENST00000350763.8:c.5125+339_5125+340delinsAC	ENSP00000265131.4:n.5125+339_5125+340delinsAC
ENST00000423613.6:c.4307-3730_4307-3729delinsAC	ENSP00000411406.2:n.4307-3730_4307-3729delinsAC
ENST00000476680.1:n.253-3730_253-3729delinsAC
ENST00000498724.5:n.40-3730_40-3729delinsAC
ENST00000535648.5:c.4036+339_4036+340delinsAC	ENSP00000438152.2:n.4036+339_4036+340delinsAC
ENST00000537320.5:c.3215-3730_3215-3729delinsAC	ENSP00000443478.1:n.3215-3730_3215-3729delinsAC
ENST00000542877.5:c.4036+339_4036+340delinsAC	ENSP00000442242.1:n.4036+339_4036+340delinsAC
ENST00000544972.1:c.812+339_812+340delinsAC
NM_002160.3:c.5125+339_5125+340delinsAC	NP_002151.2:n.5125+339_5125+340delinsAC
XM_005251972.2:c.4852+339_4852+340delinsAC	XP_005252029.1:n.4852+339_4852+340delinsAC
XM_005251973.2:c.4034-3730_4034-3729delinsAC	XP_005252030.1:n.4034-3730_4034-3729delinsAC
XM_005251974.2:c.3487+339_3487+340delinsAC	XP_005252031.1:n.3487+339_3487+340delinsAC
XM_005251975.2:c.3215-3730_3215-3729delinsAC	XP_005252032.1:n.3215-3730_3215-3729delinsAC
XM_006717096.2:c.5401+339_5401+340delinsAC	XP_006717159.1:n.5401+339_5401+340delinsAC
XM_006717097.2:c.4852+339_4852+340delinsAC	XP_006717160.1:n.4852+339_4852+340delinsAC
XM_006717098.2:c.4579+339_4579+340delinsAC	XP_006717161.1:n.4579+339_4579+340delinsAC
XM_006717100.2:c.4307-3730_4307-3729delinsAC	XP_006717163.1:n.4307-3730_4307-3729delinsAC
XM_006717101.2:c.3488-3730_3488-3729delinsAC	XP_006717164.1:n.3488-3730_3488-3729delinsAC
XM_011518622.1:c.5128+339_5128+340delinsAC	XP_011516924.1:n.5128+339_5128+340delinsAC
XM_011518623.1:c.5128+339_5128+340delinsAC	XP_011516925.1:n.5128+339_5128+340delinsAC
XM_011518624.1:c.4582+339_4582+340delinsAC	XP_011516926.1:n.4582+339_4582+340delinsAC
XM_011518625.1:c.4580-3730_4580-3729delinsAC	XP_011516927.1:n.4580-3730_4580-3729delinsAC
XM_011518626.1:c.4309+339_4309+340delinsAC	XP_011516928.1:n.4309+339_4309+340delinsAC
XM_011518627.1:c.4036+339_4036+340delinsAC	XP_011516929.1:n.4036+339_4036+340delinsAC
XM_011518628.1:c.3761-3730_3761-3729delinsAC	XP_011516930.1:n.3761-3730_3761-3729delinsAC
XM_011518629.1:c.3760+339_3760+340delinsAC	XP_011516931.1:n.3760+339_3760+340delinsAC
XM_005251972.4:c.4852+339_4852+340delinsAC	XP_005252029.1:n.4852+339_4852+340delinsAC
XM_005251973.4:c.4034-3730_4034-3729delinsAC	XP_005252030.1:n.4034-3730_4034-3729delinsAC
XM_005251974.4:c.3487+339_3487+340delinsAC	XP_005252031.1:n.3487+339_3487+340delinsAC
XM_005251975.4:c.3215-3730_3215-3729delinsAC	XP_005252032.1:n.3215-3730_3215-3729delinsAC
XM_006717096.4:c.5401+339_5401+340delinsAC	XP_006717159.1:n.5401+339_5401+340delinsAC
XM_006717097.4:c.4852+339_4852+340delinsAC	XP_006717160.1:n.4852+339_4852+340delinsAC
XM_006717098.4:c.4579+339_4579+340delinsAC	XP_006717161.1:n.4579+339_4579+340delinsAC
XM_006717101.4:c.3488-3730_3488-3729delinsAC	XP_006717164.1:n.3488-3730_3488-3729delinsAC
XM_011518625.3:c.4580-3730_4580-3729delinsAC	XP_011516927.1:n.4580-3730_4580-3729delinsAC
XM_011518626.3:c.4309+339_4309+340delinsAC	XP_011516928.1:n.4309+339_4309+340delinsAC
XM_011518628.3:c.3761-3730_3761-3729delinsAC	XP_011516930.1:n.3761-3730_3761-3729delinsAC
XM_011518629.3:c.3760+339_3760+340delinsAC	XP_011516931.1:n.3760+339_3760+340delinsAC
XM_017014678.2:c.5674+339_5674+340delinsAC	XP_016870167.1:n.5674+339_5674+340delinsAC
XM_017014679.2:c.5401+339_5401+340delinsAC	XP_016870168.1:n.5401+339_5401+340delinsAC
XM_017014680.2:c.5398+339_5398+340delinsAC	XP_016870169.1:n.5398+339_5398+340delinsAC
XM_017014681.2:c.4582+339_4582+340delinsAC	XP_016870170.1:n.4582+339_4582+340delinsAC
XM_024447530.1:c.5674+339_5674+340delinsAC	XP_024303298.1:n.5674+339_5674+340delinsAC
NM_002160.4:c.5125+339_5125+340delinsAC MANE Select	NP_002151.2:n.5125+339_5125+340delinsAC