Canonical Allele Identifier: CA2691393440

Gene: TNC

Linked Data

• gnomAD v4: 9-115046301-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115046304_115046305del , CM000671.2:g.115046304_115046305del	GRCh38
NC_000009.11:g.117808583_117808584del , CM000671.1:g.117808583_117808584del	GRCh37
NC_000009.10:g.116848404_116848405del	NCBI36
NG_029637.1:g.76955_76956del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476680.2:c.318-3962_318-3961del
ENST00000537320.6:c.3215-3962_3215-3961del	ENSP00000443478.1:n.3215-3962_3215-3961del
ENST00000542877.6:c.4036+107_4036+108del	ENSP00000442242.1:n.4036+107_4036+108del
ENST00000705190.1:c.2068+107_2068+108del	ENSP00000516083.1:n.2068+107_2068+108del
ENST00000705191.1:c.724+107_724+108del	ENSP00000516084.1:n.724+107_724+108del
ENST00000705192.1:c.4083+107_4083+108del
ENST00000350763.9:c.5125+107_5125+108del MANE Select	ENSP00000265131.4:n.5125+107_5125+108del
ENST00000341037.8:c.4579+107_4579+108del	ENSP00000339553.4:n.4579+107_4579+108del
ENST00000350763.8:c.5125+107_5125+108del	ENSP00000265131.4:n.5125+107_5125+108del
ENST00000423613.6:c.4307-3962_4307-3961del	ENSP00000411406.2:n.4307-3962_4307-3961del
ENST00000476680.1:n.253-3962_253-3961del
ENST00000498724.5:n.40-3962_40-3961del
ENST00000535648.5:c.4036+107_4036+108del	ENSP00000438152.2:n.4036+107_4036+108del
ENST00000537320.5:c.3215-3962_3215-3961del	ENSP00000443478.1:n.3215-3962_3215-3961del
ENST00000542877.5:c.4036+107_4036+108del	ENSP00000442242.1:n.4036+107_4036+108del
ENST00000544972.1:c.812+107_812+108del
NM_002160.3:c.5125+107_5125+108del	NP_002151.2:n.5125+107_5125+108del
XM_005251972.2:c.4852+107_4852+108del	XP_005252029.1:n.4852+107_4852+108del
XM_005251973.2:c.4034-3962_4034-3961del	XP_005252030.1:n.4034-3962_4034-3961del
XM_005251974.2:c.3487+107_3487+108del	XP_005252031.1:n.3487+107_3487+108del
XM_005251975.2:c.3215-3962_3215-3961del	XP_005252032.1:n.3215-3962_3215-3961del
XM_006717096.2:c.5401+107_5401+108del	XP_006717159.1:n.5401+107_5401+108del
XM_006717097.2:c.4852+107_4852+108del	XP_006717160.1:n.4852+107_4852+108del
XM_006717098.2:c.4579+107_4579+108del	XP_006717161.1:n.4579+107_4579+108del
XM_006717100.2:c.4307-3962_4307-3961del	XP_006717163.1:n.4307-3962_4307-3961del
XM_006717101.2:c.3488-3962_3488-3961del	XP_006717164.1:n.3488-3962_3488-3961del
XM_011518622.1:c.5128+107_5128+108del	XP_011516924.1:n.5128+107_5128+108del
XM_011518623.1:c.5128+107_5128+108del	XP_011516925.1:n.5128+107_5128+108del
XM_011518624.1:c.4582+107_4582+108del	XP_011516926.1:n.4582+107_4582+108del
XM_011518625.1:c.4580-3962_4580-3961del	XP_011516927.1:n.4580-3962_4580-3961del
XM_011518626.1:c.4309+107_4309+108del	XP_011516928.1:n.4309+107_4309+108del
XM_011518627.1:c.4036+107_4036+108del	XP_011516929.1:n.4036+107_4036+108del
XM_011518628.1:c.3761-3962_3761-3961del	XP_011516930.1:n.3761-3962_3761-3961del
XM_011518629.1:c.3760+107_3760+108del	XP_011516931.1:n.3760+107_3760+108del
XM_005251972.4:c.4852+107_4852+108del	XP_005252029.1:n.4852+107_4852+108del
XM_005251973.4:c.4034-3962_4034-3961del	XP_005252030.1:n.4034-3962_4034-3961del
XM_005251974.4:c.3487+107_3487+108del	XP_005252031.1:n.3487+107_3487+108del
XM_005251975.4:c.3215-3962_3215-3961del	XP_005252032.1:n.3215-3962_3215-3961del
XM_006717096.4:c.5401+107_5401+108del	XP_006717159.1:n.5401+107_5401+108del
XM_006717097.4:c.4852+107_4852+108del	XP_006717160.1:n.4852+107_4852+108del
XM_006717098.4:c.4579+107_4579+108del	XP_006717161.1:n.4579+107_4579+108del
XM_006717101.4:c.3488-3962_3488-3961del	XP_006717164.1:n.3488-3962_3488-3961del
XM_011518625.3:c.4580-3962_4580-3961del	XP_011516927.1:n.4580-3962_4580-3961del
XM_011518626.3:c.4309+107_4309+108del	XP_011516928.1:n.4309+107_4309+108del
XM_011518628.3:c.3761-3962_3761-3961del	XP_011516930.1:n.3761-3962_3761-3961del
XM_011518629.3:c.3760+107_3760+108del	XP_011516931.1:n.3760+107_3760+108del
XM_017014678.2:c.5674+107_5674+108del	XP_016870167.1:n.5674+107_5674+108del
XM_017014679.2:c.5401+107_5401+108del	XP_016870168.1:n.5401+107_5401+108del
XM_017014680.2:c.5398+107_5398+108del	XP_016870169.1:n.5398+107_5398+108del
XM_017014681.2:c.4582+107_4582+108del	XP_016870170.1:n.4582+107_4582+108del
XM_024447530.1:c.5674+107_5674+108del	XP_024303298.1:n.5674+107_5674+108del
NM_002160.4:c.5125+107_5125+108del MANE Select	NP_002151.2:n.5125+107_5125+108del