Canonical Allele Identifier: CA374631103

Gene: TNC

Linked Data

• dbSNP Id: rs1831209897
• gnomAD v3: 9-115046570-T-A
• gnomAD v4: 9-115046570-T-A
• MyVariant Identifiers: chr9:g.117808849T>A (hg19) ; chr9:g.115046570T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115046570T>A , CM000671.2:g.115046570T>A	GRCh38
NC_000009.11:g.117808849T>A , CM000671.1:g.117808849T>A	GRCh37
NC_000009.10:g.116848670T>A	NCBI36
NG_029637.1:g.76688A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476680.2:c.318-4229A>T
ENST00000537320.6:c.3215-4229A>T	ENSP00000443478.1:n.3215-4229A>T
ENST00000542877.6:c.3876A>T	ENSP00000442242.1:p.Arg1292Ser
ENST00000705190.1:c.1908A>T	ENSP00000516083.1:p.Arg636Ser
ENST00000705191.1:c.564A>T	ENSP00000516084.1:p.Arg188Ser
ENST00000705192.1:c.3923A>T
ENST00000350763.9:c.4965A>T MANE Select	ENSP00000265131.4:p.Arg1655Ser
ENST00000341037.8:c.4419A>T	ENSP00000339553.4:p.Arg1473Ser
ENST00000350763.8:c.4965A>T	ENSP00000265131.4:p.Arg1655Ser
ENST00000423613.6:c.4307-4229A>T	ENSP00000411406.2:n.4307-4229A>T
ENST00000473855.1:n.283A>T
ENST00000476680.1:n.253-4229A>T
ENST00000498724.5:n.40-4229A>T
ENST00000535648.5:c.3876A>T	ENSP00000438152.2:p.Arg1292Ser
ENST00000537320.5:c.3215-4229A>T	ENSP00000443478.1:n.3215-4229A>T
ENST00000542877.5:c.3876A>T	ENSP00000442242.1:p.Arg1292Ser
ENST00000544972.1:c.652A>T
NM_002160.3:c.4965A>T	NP_002151.2:p.Arg1655Ser
XM_005251972.2:c.4692A>T	XP_005252029.1:p.Arg1564Ser
XM_005251973.2:c.4034-4229A>T	XP_005252030.1:n.4034-4229A>T
XM_005251974.2:c.3327A>T	XP_005252031.1:p.Arg1109Ser
XM_005251975.2:c.3215-4229A>T	XP_005252032.1:n.3215-4229A>T
XM_006717096.2:c.5241A>T	XP_006717159.1:p.Arg1747Ser
XM_006717097.2:c.4692A>T	XP_006717160.1:p.Arg1564Ser
XM_006717098.2:c.4419A>T	XP_006717161.1:p.Arg1473Ser
XM_006717100.2:c.4307-4229A>T	XP_006717163.1:n.4307-4229A>T
XM_006717101.2:c.3488-4229A>T	XP_006717164.1:n.3488-4229A>T
XM_011518622.1:c.4968A>T	XP_011516924.1:p.Arg1656Ser
XM_011518623.1:c.4968A>T	XP_011516925.1:p.Arg1656Ser
XM_011518624.1:c.4422A>T	XP_011516926.1:p.Arg1474Ser
XM_011518625.1:c.4580-4229A>T	XP_011516927.1:n.4580-4229A>T
XM_011518626.1:c.4149A>T	XP_011516928.1:p.Arg1383Ser
XM_011518627.1:c.3876A>T	XP_011516929.1:p.Arg1292Ser
XM_011518628.1:c.3761-4229A>T	XP_011516930.1:n.3761-4229A>T
XM_011518629.1:c.3600A>T	XP_011516931.1:p.Arg1200Ser
XM_005251972.4:c.4692A>T	XP_005252029.1:p.Arg1564Ser
XM_005251973.4:c.4034-4229A>T	XP_005252030.1:n.4034-4229A>T
XM_005251974.4:c.3327A>T	XP_005252031.1:p.Arg1109Ser
XM_005251975.4:c.3215-4229A>T	XP_005252032.1:n.3215-4229A>T
XM_006717096.4:c.5241A>T	XP_006717159.1:p.Arg1747Ser
XM_006717097.4:c.4692A>T	XP_006717160.1:p.Arg1564Ser
XM_006717098.4:c.4419A>T	XP_006717161.1:p.Arg1473Ser
XM_006717101.4:c.3488-4229A>T	XP_006717164.1:n.3488-4229A>T
XM_011518625.3:c.4580-4229A>T	XP_011516927.1:n.4580-4229A>T
XM_011518626.3:c.4149A>T	XP_011516928.1:p.Arg1383Ser
XM_011518628.3:c.3761-4229A>T	XP_011516930.1:n.3761-4229A>T
XM_011518629.3:c.3600A>T	XP_011516931.1:p.Arg1200Ser
XM_017014678.2:c.5514A>T	XP_016870167.1:p.Arg1838Ser
XM_017014679.2:c.5241A>T	XP_016870168.1:p.Arg1747Ser
XM_017014680.2:c.5238A>T	XP_016870169.1:p.Arg1746Ser
XM_017014681.2:c.4422A>T	XP_016870170.1:p.Arg1474Ser
XM_024447530.1:c.5514A>T	XP_024303298.1:p.Arg1838Ser
NM_002160.4:c.4965A>T MANE Select	NP_002151.2:p.Arg1655Ser