Canonical Allele Identifier: CA2691393278

Gene: TNC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115042104_115042107del , CM000671.2:g.115042104_115042107del	GRCh38
NC_000009.11:g.117804383_117804386del , CM000671.1:g.117804383_117804386del	GRCh37
NC_000009.10:g.116844204_116844207del	NCBI36
NG_029637.1:g.81153_81156del

Transcript Alleles

HGVS	Amino-acid Change
NM_002160.4:c.5248+114_5248+117del MANE Select	NP_002151.2:n.5248+114_5248+117del
ENST00000350763.9:c.5248+114_5248+117del MANE Select	ENSP00000265131.4:n.5248+114_5248+117del
NM_002160.3:c.5248+114_5248+117del	NP_002151.2:n.5248+114_5248+117del
ENST00000341037.8:c.4702+114_4702+117del	ENSP00000339553.4:n.4702+114_4702+117del
ENST00000350763.8:c.5248+114_5248+117del	ENSP00000265131.4:n.5248+114_5248+117del
ENST00000423613.6:c.4429+114_4429+117del	ENSP00000411406.2:n.4429+114_4429+117del
ENST00000476680.1:n.375+114_375+117del
ENST00000476680.2:c.440+114_440+117del
ENST00000498724.5:n.162+114_162+117del
ENST00000535648.5:c.4159+114_4159+117del	ENSP00000438152.2:n.4159+114_4159+117del
ENST00000537320.5:c.3337+114_3337+117del	ENSP00000443478.1:n.3337+114_3337+117del
ENST00000537320.6:c.3337+114_3337+117del	ENSP00000443478.1:n.3337+114_3337+117del
ENST00000542877.5:c.4159+114_4159+117del	ENSP00000442242.1:n.4159+114_4159+117del
ENST00000542877.6:c.4159+114_4159+117del	ENSP00000442242.1:n.4159+114_4159+117del
ENST00000544972.1:c.935+114_935+117del
ENST00000705190.1:c.2191+114_2191+117del	ENSP00000516083.1:n.2191+114_2191+117del
ENST00000705191.1:c.847+114_847+117del	ENSP00000516084.1:n.847+114_847+117del
ENST00000705192.1:c.4206+114_4206+117del
XM_005251972.2:c.4975+114_4975+117del	XP_005252029.1:n.4975+114_4975+117del
XM_005251972.4:c.4975+114_4975+117del	XP_005252029.1:n.4975+114_4975+117del
XM_005251973.2:c.4156+114_4156+117del	XP_005252030.1:n.4156+114_4156+117del
XM_005251973.4:c.4156+114_4156+117del	XP_005252030.1:n.4156+114_4156+117del
XM_005251974.2:c.3610+114_3610+117del	XP_005252031.1:n.3610+114_3610+117del
XM_005251974.4:c.3610+114_3610+117del	XP_005252031.1:n.3610+114_3610+117del
XM_005251975.2:c.3337+114_3337+117del	XP_005252032.1:n.3337+114_3337+117del
XM_005251975.4:c.3337+114_3337+117del	XP_005252032.1:n.3337+114_3337+117del
XM_006717096.2:c.5524+114_5524+117del	XP_006717159.1:n.5524+114_5524+117del
XM_006717096.4:c.5524+114_5524+117del	XP_006717159.1:n.5524+114_5524+117del
XM_006717097.2:c.4975+114_4975+117del	XP_006717160.1:n.4975+114_4975+117del
XM_006717097.4:c.4975+114_4975+117del	XP_006717160.1:n.4975+114_4975+117del
XM_006717098.2:c.4702+114_4702+117del	XP_006717161.1:n.4702+114_4702+117del
XM_006717098.4:c.4702+114_4702+117del	XP_006717161.1:n.4702+114_4702+117del
XM_006717100.2:c.4429+114_4429+117del	XP_006717163.1:n.4429+114_4429+117del
XM_006717101.2:c.3610+114_3610+117del	XP_006717164.1:n.3610+114_3610+117del
XM_006717101.4:c.3610+114_3610+117del	XP_006717164.1:n.3610+114_3610+117del
XM_011518622.1:c.5251+114_5251+117del	XP_011516924.1:n.5251+114_5251+117del
XM_011518623.1:c.5251+114_5251+117del	XP_011516925.1:n.5251+114_5251+117del
XM_011518624.1:c.4705+114_4705+117del	XP_011516926.1:n.4705+114_4705+117del
XM_011518625.1:c.4702+114_4702+117del	XP_011516927.1:n.4702+114_4702+117del
XM_011518625.3:c.4702+114_4702+117del	XP_011516927.1:n.4702+114_4702+117del
XM_011518626.1:c.4432+114_4432+117del	XP_011516928.1:n.4432+114_4432+117del
XM_011518626.3:c.4432+114_4432+117del	XP_011516928.1:n.4432+114_4432+117del
XM_011518627.1:c.4159+114_4159+117del	XP_011516929.1:n.4159+114_4159+117del
XM_011518628.1:c.3883+114_3883+117del	XP_011516930.1:n.3883+114_3883+117del
XM_011518628.3:c.3883+114_3883+117del	XP_011516930.1:n.3883+114_3883+117del
XM_011518629.1:c.3883+114_3883+117del	XP_011516931.1:n.3883+114_3883+117del
XM_011518629.3:c.3883+114_3883+117del	XP_011516931.1:n.3883+114_3883+117del
XM_017014678.2:c.5797+114_5797+117del	XP_016870167.1:n.5797+114_5797+117del
XM_017014679.2:c.5524+114_5524+117del	XP_016870168.1:n.5524+114_5524+117del
XM_017014680.2:c.5521+114_5521+117del	XP_016870169.1:n.5521+114_5521+117del
XM_017014681.2:c.4705+114_4705+117del	XP_016870170.1:n.4705+114_4705+117del
XM_024447530.1:c.5797+114_5797+117del	XP_024303298.1:n.5797+114_5797+117del