Canonical Allele Identifier: CA2691393426
Gene: TNC HGNC NCBI

Linked Data

gnomAD v4: 9-115046287-GAA-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.115046289_115046290del , CM000671.2:g.115046289_115046290del GRCh38
NC_000009.11:g.117808568_117808569del , CM000671.1:g.117808568_117808569del GRCh37
NC_000009.10:g.116848389_116848390del NCBI36
NG_029637.1:g.76969_76970del

Transcript Alleles

HGVS Amino-acid Change
ENST00000476680.2:c.318-3948_318-3947del
ENST00000537320.6:c.3215-3948_3215-3947del ENSP00000443478.1:n.3215-3948_3215-3947del
ENST00000542877.6:c.4036+121_4036+122del ENSP00000442242.1:n.4036+121_4036+122del
ENST00000705190.1:c.2068+121_2068+122del ENSP00000516083.1:n.2068+121_2068+122del
ENST00000705191.1:c.724+121_724+122del ENSP00000516084.1:n.724+121_724+122del
ENST00000705192.1:c.4083+121_4083+122del
ENST00000350763.9:c.5125+121_5125+122del MANE Select ENSP00000265131.4:n.5125+121_5125+122del
ENST00000341037.8:c.4579+121_4579+122del ENSP00000339553.4:n.4579+121_4579+122del
ENST00000350763.8:c.5125+121_5125+122del ENSP00000265131.4:n.5125+121_5125+122del
ENST00000423613.6:c.4307-3948_4307-3947del ENSP00000411406.2:n.4307-3948_4307-3947del
ENST00000476680.1:n.253-3948_253-3947del
ENST00000498724.5:n.40-3948_40-3947del
ENST00000535648.5:c.4036+121_4036+122del ENSP00000438152.2:n.4036+121_4036+122del
ENST00000537320.5:c.3215-3948_3215-3947del ENSP00000443478.1:n.3215-3948_3215-3947del
ENST00000542877.5:c.4036+121_4036+122del ENSP00000442242.1:n.4036+121_4036+122del
ENST00000544972.1:c.812+121_812+122del
NM_002160.3:c.5125+121_5125+122del NP_002151.2:n.5125+121_5125+122del
XM_005251972.2:c.4852+121_4852+122del XP_005252029.1:n.4852+121_4852+122del
XM_005251973.2:c.4034-3948_4034-3947del XP_005252030.1:n.4034-3948_4034-3947del
XM_005251974.2:c.3487+121_3487+122del XP_005252031.1:n.3487+121_3487+122del
XM_005251975.2:c.3215-3948_3215-3947del XP_005252032.1:n.3215-3948_3215-3947del
XM_006717096.2:c.5401+121_5401+122del XP_006717159.1:n.5401+121_5401+122del
XM_006717097.2:c.4852+121_4852+122del XP_006717160.1:n.4852+121_4852+122del
XM_006717098.2:c.4579+121_4579+122del XP_006717161.1:n.4579+121_4579+122del
XM_006717100.2:c.4307-3948_4307-3947del XP_006717163.1:n.4307-3948_4307-3947del
XM_006717101.2:c.3488-3948_3488-3947del XP_006717164.1:n.3488-3948_3488-3947del
XM_011518622.1:c.5128+121_5128+122del XP_011516924.1:n.5128+121_5128+122del
XM_011518623.1:c.5128+121_5128+122del XP_011516925.1:n.5128+121_5128+122del
XM_011518624.1:c.4582+121_4582+122del XP_011516926.1:n.4582+121_4582+122del
XM_011518625.1:c.4580-3948_4580-3947del XP_011516927.1:n.4580-3948_4580-3947del
XM_011518626.1:c.4309+121_4309+122del XP_011516928.1:n.4309+121_4309+122del
XM_011518627.1:c.4036+121_4036+122del XP_011516929.1:n.4036+121_4036+122del
XM_011518628.1:c.3761-3948_3761-3947del XP_011516930.1:n.3761-3948_3761-3947del
XM_011518629.1:c.3760+121_3760+122del XP_011516931.1:n.3760+121_3760+122del
XM_005251972.4:c.4852+121_4852+122del XP_005252029.1:n.4852+121_4852+122del
XM_005251973.4:c.4034-3948_4034-3947del XP_005252030.1:n.4034-3948_4034-3947del
XM_005251974.4:c.3487+121_3487+122del XP_005252031.1:n.3487+121_3487+122del
XM_005251975.4:c.3215-3948_3215-3947del XP_005252032.1:n.3215-3948_3215-3947del
XM_006717096.4:c.5401+121_5401+122del XP_006717159.1:n.5401+121_5401+122del
XM_006717097.4:c.4852+121_4852+122del XP_006717160.1:n.4852+121_4852+122del
XM_006717098.4:c.4579+121_4579+122del XP_006717161.1:n.4579+121_4579+122del
XM_006717101.4:c.3488-3948_3488-3947del XP_006717164.1:n.3488-3948_3488-3947del
XM_011518625.3:c.4580-3948_4580-3947del XP_011516927.1:n.4580-3948_4580-3947del
XM_011518626.3:c.4309+121_4309+122del XP_011516928.1:n.4309+121_4309+122del
XM_011518628.3:c.3761-3948_3761-3947del XP_011516930.1:n.3761-3948_3761-3947del
XM_011518629.3:c.3760+121_3760+122del XP_011516931.1:n.3760+121_3760+122del
XM_017014678.2:c.5674+121_5674+122del XP_016870167.1:n.5674+121_5674+122del
XM_017014679.2:c.5401+121_5401+122del XP_016870168.1:n.5401+121_5401+122del
XM_017014680.2:c.5398+121_5398+122del XP_016870169.1:n.5398+121_5398+122del
XM_017014681.2:c.4582+121_4582+122del XP_016870170.1:n.4582+121_4582+122del
XM_024447530.1:c.5674+121_5674+122del XP_024303298.1:n.5674+121_5674+122del
NM_002160.4:c.5125+121_5125+122del MANE Select NP_002151.2:n.5125+121_5125+122del
Search 100 bp 5'
Search 100 bp 3'