Canonical Allele Identifier: CA374630903

Gene: TNC

Linked Data

• ClinVar Variation Id: 2252203
• ClinVar RCV Id: RCV004109907
• dbSNP Id: rs1831204887
• MyVariant Identifiers: chr9:g.117808793G>C (hg19) ; chr9:g.115046514G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115046514G>C , CM000671.2:g.115046514G>C	GRCh38
NC_000009.11:g.117808793G>C , CM000671.1:g.117808793G>C	GRCh37
NC_000009.10:g.116848614G>C	NCBI36
NG_029637.1:g.76744C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476680.2:c.318-4173C>G
ENST00000537320.6:c.3215-4173C>G	ENSP00000443478.1:n.3215-4173C>G
ENST00000542877.6:c.3932C>G	ENSP00000442242.1:p.Thr1311Ser
ENST00000705190.1:c.1964C>G	ENSP00000516083.1:p.Thr655Ser
ENST00000705191.1:c.620C>G	ENSP00000516084.1:p.Thr207Ser
ENST00000705192.1:c.3979C>G
ENST00000350763.9:c.5021C>G MANE Select	ENSP00000265131.4:p.Thr1674Ser
ENST00000341037.8:c.4475C>G	ENSP00000339553.4:p.Thr1492Ser
ENST00000350763.8:c.5021C>G	ENSP00000265131.4:p.Thr1674Ser
ENST00000423613.6:c.4307-4173C>G	ENSP00000411406.2:n.4307-4173C>G
ENST00000473855.1:n.339C>G
ENST00000476680.1:n.253-4173C>G
ENST00000498724.5:n.40-4173C>G
ENST00000535648.5:c.3932C>G	ENSP00000438152.2:p.Thr1311Ser
ENST00000537320.5:c.3215-4173C>G	ENSP00000443478.1:n.3215-4173C>G
ENST00000542877.5:c.3932C>G	ENSP00000442242.1:p.Thr1311Ser
ENST00000544972.1:c.708C>G
NM_002160.3:c.5021C>G	NP_002151.2:p.Thr1674Ser
XM_005251972.2:c.4748C>G	XP_005252029.1:p.Thr1583Ser
XM_005251973.2:c.4034-4173C>G	XP_005252030.1:n.4034-4173C>G
XM_005251974.2:c.3383C>G	XP_005252031.1:p.Thr1128Ser
XM_005251975.2:c.3215-4173C>G	XP_005252032.1:n.3215-4173C>G
XM_006717096.2:c.5297C>G	XP_006717159.1:p.Thr1766Ser
XM_006717097.2:c.4748C>G	XP_006717160.1:p.Thr1583Ser
XM_006717098.2:c.4475C>G	XP_006717161.1:p.Thr1492Ser
XM_006717100.2:c.4307-4173C>G	XP_006717163.1:n.4307-4173C>G
XM_006717101.2:c.3488-4173C>G	XP_006717164.1:n.3488-4173C>G
XM_011518622.1:c.5024C>G	XP_011516924.1:p.Thr1675Ser
XM_011518623.1:c.5024C>G	XP_011516925.1:p.Thr1675Ser
XM_011518624.1:c.4478C>G	XP_011516926.1:p.Thr1493Ser
XM_011518625.1:c.4580-4173C>G	XP_011516927.1:n.4580-4173C>G
XM_011518626.1:c.4205C>G	XP_011516928.1:p.Thr1402Ser
XM_011518627.1:c.3932C>G	XP_011516929.1:p.Thr1311Ser
XM_011518628.1:c.3761-4173C>G	XP_011516930.1:n.3761-4173C>G
XM_011518629.1:c.3656C>G	XP_011516931.1:p.Thr1219Ser
XM_005251972.4:c.4748C>G	XP_005252029.1:p.Thr1583Ser
XM_005251973.4:c.4034-4173C>G	XP_005252030.1:n.4034-4173C>G
XM_005251974.4:c.3383C>G	XP_005252031.1:p.Thr1128Ser
XM_005251975.4:c.3215-4173C>G	XP_005252032.1:n.3215-4173C>G
XM_006717096.4:c.5297C>G	XP_006717159.1:p.Thr1766Ser
XM_006717097.4:c.4748C>G	XP_006717160.1:p.Thr1583Ser
XM_006717098.4:c.4475C>G	XP_006717161.1:p.Thr1492Ser
XM_006717101.4:c.3488-4173C>G	XP_006717164.1:n.3488-4173C>G
XM_011518625.3:c.4580-4173C>G	XP_011516927.1:n.4580-4173C>G
XM_011518626.3:c.4205C>G	XP_011516928.1:p.Thr1402Ser
XM_011518628.3:c.3761-4173C>G	XP_011516930.1:n.3761-4173C>G
XM_011518629.3:c.3656C>G	XP_011516931.1:p.Thr1219Ser
XM_017014678.2:c.5570C>G	XP_016870167.1:p.Thr1857Ser
XM_017014679.2:c.5297C>G	XP_016870168.1:p.Thr1766Ser
XM_017014680.2:c.5294C>G	XP_016870169.1:p.Thr1765Ser
XM_017014681.2:c.4478C>G	XP_016870170.1:p.Thr1493Ser
XM_024447530.1:c.5570C>G	XP_024303298.1:p.Thr1857Ser
NM_002160.4:c.5021C>G MANE Select	NP_002151.2:p.Thr1674Ser