Canonical Allele Identifier: CA918540848

Gene: TNC

Linked Data

• dbSNP Id: rs1588049786

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115046043_115046045del , CM000671.2:g.115046043_115046045del	GRCh38
NC_000009.11:g.117808322_117808324del , CM000671.1:g.117808322_117808324del	GRCh37
NC_000009.10:g.116848143_116848145del	NCBI36
NG_029637.1:g.77216_77218del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476680.2:c.318-3701_318-3699del
ENST00000537320.6:c.3215-3701_3215-3699del	ENSP00000443478.1:n.3215-3701_3215-3699del
ENST00000542877.6:c.4036+368_4036+370del	ENSP00000442242.1:n.4036+368_4036+370del
ENST00000705190.1:c.2068+368_2068+370del	ENSP00000516083.1:n.2068+368_2068+370del
ENST00000705191.1:c.724+368_724+370del	ENSP00000516084.1:n.724+368_724+370del
ENST00000705192.1:c.4083+368_4083+370del
ENST00000350763.9:c.5125+368_5125+370del MANE Select	ENSP00000265131.4:n.5125+368_5125+370del
ENST00000341037.8:c.4579+368_4579+370del	ENSP00000339553.4:n.4579+368_4579+370del
ENST00000350763.8:c.5125+368_5125+370del	ENSP00000265131.4:n.5125+368_5125+370del
ENST00000423613.6:c.4307-3701_4307-3699del	ENSP00000411406.2:n.4307-3701_4307-3699del
ENST00000476680.1:n.253-3701_253-3699del
ENST00000498724.5:n.40-3701_40-3699del
ENST00000535648.5:c.4036+368_4036+370del	ENSP00000438152.2:n.4036+368_4036+370del
ENST00000537320.5:c.3215-3701_3215-3699del	ENSP00000443478.1:n.3215-3701_3215-3699del
ENST00000542877.5:c.4036+368_4036+370del	ENSP00000442242.1:n.4036+368_4036+370del
ENST00000544972.1:c.812+368_812+370del
NM_002160.3:c.5125+368_5125+370del	NP_002151.2:n.5125+368_5125+370del
XM_005251972.2:c.4852+368_4852+370del	XP_005252029.1:n.4852+368_4852+370del
XM_005251973.2:c.4034-3701_4034-3699del	XP_005252030.1:n.4034-3701_4034-3699del
XM_005251974.2:c.3487+368_3487+370del	XP_005252031.1:n.3487+368_3487+370del
XM_005251975.2:c.3215-3701_3215-3699del	XP_005252032.1:n.3215-3701_3215-3699del
XM_006717096.2:c.5401+368_5401+370del	XP_006717159.1:n.5401+368_5401+370del
XM_006717097.2:c.4852+368_4852+370del	XP_006717160.1:n.4852+368_4852+370del
XM_006717098.2:c.4579+368_4579+370del	XP_006717161.1:n.4579+368_4579+370del
XM_006717100.2:c.4307-3701_4307-3699del	XP_006717163.1:n.4307-3701_4307-3699del
XM_006717101.2:c.3488-3701_3488-3699del	XP_006717164.1:n.3488-3701_3488-3699del
XM_011518622.1:c.5128+368_5128+370del	XP_011516924.1:n.5128+368_5128+370del
XM_011518623.1:c.5128+368_5128+370del	XP_011516925.1:n.5128+368_5128+370del
XM_011518624.1:c.4582+368_4582+370del	XP_011516926.1:n.4582+368_4582+370del
XM_011518625.1:c.4580-3701_4580-3699del	XP_011516927.1:n.4580-3701_4580-3699del
XM_011518626.1:c.4309+368_4309+370del	XP_011516928.1:n.4309+368_4309+370del
XM_011518627.1:c.4036+368_4036+370del	XP_011516929.1:n.4036+368_4036+370del
XM_011518628.1:c.3761-3701_3761-3699del	XP_011516930.1:n.3761-3701_3761-3699del
XM_011518629.1:c.3760+368_3760+370del	XP_011516931.1:n.3760+368_3760+370del
XM_005251972.4:c.4852+368_4852+370del	XP_005252029.1:n.4852+368_4852+370del
XM_005251973.4:c.4034-3701_4034-3699del	XP_005252030.1:n.4034-3701_4034-3699del
XM_005251974.4:c.3487+368_3487+370del	XP_005252031.1:n.3487+368_3487+370del
XM_005251975.4:c.3215-3701_3215-3699del	XP_005252032.1:n.3215-3701_3215-3699del
XM_006717096.4:c.5401+368_5401+370del	XP_006717159.1:n.5401+368_5401+370del
XM_006717097.4:c.4852+368_4852+370del	XP_006717160.1:n.4852+368_4852+370del
XM_006717098.4:c.4579+368_4579+370del	XP_006717161.1:n.4579+368_4579+370del
XM_006717101.4:c.3488-3701_3488-3699del	XP_006717164.1:n.3488-3701_3488-3699del
XM_011518625.3:c.4580-3701_4580-3699del	XP_011516927.1:n.4580-3701_4580-3699del
XM_011518626.3:c.4309+368_4309+370del	XP_011516928.1:n.4309+368_4309+370del
XM_011518628.3:c.3761-3701_3761-3699del	XP_011516930.1:n.3761-3701_3761-3699del
XM_011518629.3:c.3760+368_3760+370del	XP_011516931.1:n.3760+368_3760+370del
XM_017014678.2:c.5674+368_5674+370del	XP_016870167.1:n.5674+368_5674+370del
XM_017014679.2:c.5401+368_5401+370del	XP_016870168.1:n.5401+368_5401+370del
XM_017014680.2:c.5398+368_5398+370del	XP_016870169.1:n.5398+368_5398+370del
XM_017014681.2:c.4582+368_4582+370del	XP_016870170.1:n.4582+368_4582+370del
XM_024447530.1:c.5674+368_5674+370del	XP_024303298.1:n.5674+368_5674+370del
NM_002160.4:c.5125+368_5125+370del MANE Select	NP_002151.2:n.5125+368_5125+370del