Canonical Allele Identifier: CA1874118695

Gene: TNC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115046042_115046046delinsAATAG , CM000671.2:g.115046042_115046046delinsAATAG	GRCh38
NC_000009.11:g.117808321_117808325delinsAATAG , CM000671.1:g.117808321_117808325delinsAATAG	GRCh37
NC_000009.10:g.116848142_116848146delinsAATAG	NCBI36
NG_029637.1:g.77212_77216delinsCTATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476680.2:c.318-3705_318-3701delinsCTATT
ENST00000537320.6:c.3215-3705_3215-3701delinsCTATT	ENSP00000443478.1:n.3215-3705_3215-3701delinsCTATT
ENST00000542877.6:c.4036+364_4036+368delinsCTATT	ENSP00000442242.1:n.4036+364_4036+368delinsCTATT
ENST00000705190.1:c.2068+364_2068+368delinsCTATT	ENSP00000516083.1:n.2068+364_2068+368delinsCTATT
ENST00000705191.1:c.724+364_724+368delinsCTATT	ENSP00000516084.1:n.724+364_724+368delinsCTATT
ENST00000705192.1:c.4083+364_4083+368delinsCTATT
ENST00000350763.9:c.5125+364_5125+368delinsCTATT MANE Select	ENSP00000265131.4:n.5125+364_5125+368delinsCTATT
ENST00000341037.8:c.4579+364_4579+368delinsCTATT	ENSP00000339553.4:n.4579+364_4579+368delinsCTATT
ENST00000350763.8:c.5125+364_5125+368delinsCTATT	ENSP00000265131.4:n.5125+364_5125+368delinsCTATT
ENST00000423613.6:c.4307-3705_4307-3701delinsCTATT	ENSP00000411406.2:n.4307-3705_4307-3701delinsCTATT
ENST00000476680.1:n.253-3705_253-3701delinsCTATT
ENST00000498724.5:n.40-3705_40-3701delinsCTATT
ENST00000535648.5:c.4036+364_4036+368delinsCTATT	ENSP00000438152.2:n.4036+364_4036+368delinsCTATT
ENST00000537320.5:c.3215-3705_3215-3701delinsCTATT	ENSP00000443478.1:n.3215-3705_3215-3701delinsCTATT
ENST00000542877.5:c.4036+364_4036+368delinsCTATT	ENSP00000442242.1:n.4036+364_4036+368delinsCTATT
ENST00000544972.1:c.812+364_812+368delinsCTATT
NM_002160.3:c.5125+364_5125+368delinsCTATT	NP_002151.2:n.5125+364_5125+368delinsCTATT
XM_005251972.2:c.4852+364_4852+368delinsCTATT	XP_005252029.1:n.4852+364_4852+368delinsCTATT
XM_005251973.2:c.4034-3705_4034-3701delinsCTATT	XP_005252030.1:n.4034-3705_4034-3701delinsCTATT
XM_005251974.2:c.3487+364_3487+368delinsCTATT	XP_005252031.1:n.3487+364_3487+368delinsCTATT
XM_005251975.2:c.3215-3705_3215-3701delinsCTATT	XP_005252032.1:n.3215-3705_3215-3701delinsCTATT
XM_006717096.2:c.5401+364_5401+368delinsCTATT	XP_006717159.1:n.5401+364_5401+368delinsCTATT
XM_006717097.2:c.4852+364_4852+368delinsCTATT	XP_006717160.1:n.4852+364_4852+368delinsCTATT
XM_006717098.2:c.4579+364_4579+368delinsCTATT	XP_006717161.1:n.4579+364_4579+368delinsCTATT
XM_006717100.2:c.4307-3705_4307-3701delinsCTATT	XP_006717163.1:n.4307-3705_4307-3701delinsCTATT
XM_006717101.2:c.3488-3705_3488-3701delinsCTATT	XP_006717164.1:n.3488-3705_3488-3701delinsCTATT
XM_011518622.1:c.5128+364_5128+368delinsCTATT	XP_011516924.1:n.5128+364_5128+368delinsCTATT
XM_011518623.1:c.5128+364_5128+368delinsCTATT	XP_011516925.1:n.5128+364_5128+368delinsCTATT
XM_011518624.1:c.4582+364_4582+368delinsCTATT	XP_011516926.1:n.4582+364_4582+368delinsCTATT
XM_011518625.1:c.4580-3705_4580-3701delinsCTATT	XP_011516927.1:n.4580-3705_4580-3701delinsCTATT
XM_011518626.1:c.4309+364_4309+368delinsCTATT	XP_011516928.1:n.4309+364_4309+368delinsCTATT
XM_011518627.1:c.4036+364_4036+368delinsCTATT	XP_011516929.1:n.4036+364_4036+368delinsCTATT
XM_011518628.1:c.3761-3705_3761-3701delinsCTATT	XP_011516930.1:n.3761-3705_3761-3701delinsCTATT
XM_011518629.1:c.3760+364_3760+368delinsCTATT	XP_011516931.1:n.3760+364_3760+368delinsCTATT
XM_005251972.4:c.4852+364_4852+368delinsCTATT	XP_005252029.1:n.4852+364_4852+368delinsCTATT
XM_005251973.4:c.4034-3705_4034-3701delinsCTATT	XP_005252030.1:n.4034-3705_4034-3701delinsCTATT
XM_005251974.4:c.3487+364_3487+368delinsCTATT	XP_005252031.1:n.3487+364_3487+368delinsCTATT
XM_005251975.4:c.3215-3705_3215-3701delinsCTATT	XP_005252032.1:n.3215-3705_3215-3701delinsCTATT
XM_006717096.4:c.5401+364_5401+368delinsCTATT	XP_006717159.1:n.5401+364_5401+368delinsCTATT
XM_006717097.4:c.4852+364_4852+368delinsCTATT	XP_006717160.1:n.4852+364_4852+368delinsCTATT
XM_006717098.4:c.4579+364_4579+368delinsCTATT	XP_006717161.1:n.4579+364_4579+368delinsCTATT
XM_006717101.4:c.3488-3705_3488-3701delinsCTATT	XP_006717164.1:n.3488-3705_3488-3701delinsCTATT
XM_011518625.3:c.4580-3705_4580-3701delinsCTATT	XP_011516927.1:n.4580-3705_4580-3701delinsCTATT
XM_011518626.3:c.4309+364_4309+368delinsCTATT	XP_011516928.1:n.4309+364_4309+368delinsCTATT
XM_011518628.3:c.3761-3705_3761-3701delinsCTATT	XP_011516930.1:n.3761-3705_3761-3701delinsCTATT
XM_011518629.3:c.3760+364_3760+368delinsCTATT	XP_011516931.1:n.3760+364_3760+368delinsCTATT
XM_017014678.2:c.5674+364_5674+368delinsCTATT	XP_016870167.1:n.5674+364_5674+368delinsCTATT
XM_017014679.2:c.5401+364_5401+368delinsCTATT	XP_016870168.1:n.5401+364_5401+368delinsCTATT
XM_017014680.2:c.5398+364_5398+368delinsCTATT	XP_016870169.1:n.5398+364_5398+368delinsCTATT
XM_017014681.2:c.4582+364_4582+368delinsCTATT	XP_016870170.1:n.4582+364_4582+368delinsCTATT
XM_024447530.1:c.5674+364_5674+368delinsCTATT	XP_024303298.1:n.5674+364_5674+368delinsCTATT
NM_002160.4:c.5125+364_5125+368delinsCTATT MANE Select	NP_002151.2:n.5125+364_5125+368delinsCTATT