Canonical Allele Identifier: CA374631113

Gene: TNC

Linked Data

• gnomAD v4: 9-115046573-G-C
• MyVariant Identifiers: chr9:g.117808852G>C (hg19) ; chr9:g.115046573G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115046573G>C , CM000671.2:g.115046573G>C	GRCh38
NC_000009.11:g.117808852G>C , CM000671.1:g.117808852G>C	GRCh37
NC_000009.10:g.116848673G>C	NCBI36
NG_029637.1:g.76685C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476680.2:c.318-4232C>G
ENST00000537320.6:c.3215-4232C>G	ENSP00000443478.1:n.3215-4232C>G
ENST00000542877.6:c.3873C>G	ENSP00000442242.1:p.Ile1291Met
ENST00000705190.1:c.1905C>G	ENSP00000516083.1:p.Ile635Met
ENST00000705191.1:c.561C>G	ENSP00000516084.1:p.Ile187Met
ENST00000705192.1:c.3920C>G
ENST00000350763.9:c.4962C>G MANE Select	ENSP00000265131.4:p.Ile1654Met
ENST00000341037.8:c.4416C>G	ENSP00000339553.4:p.Ile1472Met
ENST00000350763.8:c.4962C>G	ENSP00000265131.4:p.Ile1654Met
ENST00000423613.6:c.4307-4232C>G	ENSP00000411406.2:n.4307-4232C>G
ENST00000473855.1:n.280C>G
ENST00000476680.1:n.253-4232C>G
ENST00000498724.5:n.40-4232C>G
ENST00000535648.5:c.3873C>G	ENSP00000438152.2:p.Ile1291Met
ENST00000537320.5:c.3215-4232C>G	ENSP00000443478.1:n.3215-4232C>G
ENST00000542877.5:c.3873C>G	ENSP00000442242.1:p.Ile1291Met
ENST00000544972.1:c.649C>G
NM_002160.3:c.4962C>G	NP_002151.2:p.Ile1654Met
XM_005251972.2:c.4689C>G	XP_005252029.1:p.Ile1563Met
XM_005251973.2:c.4034-4232C>G	XP_005252030.1:n.4034-4232C>G
XM_005251974.2:c.3324C>G	XP_005252031.1:p.Ile1108Met
XM_005251975.2:c.3215-4232C>G	XP_005252032.1:n.3215-4232C>G
XM_006717096.2:c.5238C>G	XP_006717159.1:p.Ile1746Met
XM_006717097.2:c.4689C>G	XP_006717160.1:p.Ile1563Met
XM_006717098.2:c.4416C>G	XP_006717161.1:p.Ile1472Met
XM_006717100.2:c.4307-4232C>G	XP_006717163.1:n.4307-4232C>G
XM_006717101.2:c.3488-4232C>G	XP_006717164.1:n.3488-4232C>G
XM_011518622.1:c.4965C>G	XP_011516924.1:p.Ile1655Met
XM_011518623.1:c.4965C>G	XP_011516925.1:p.Ile1655Met
XM_011518624.1:c.4419C>G	XP_011516926.1:p.Ile1473Met
XM_011518625.1:c.4580-4232C>G	XP_011516927.1:n.4580-4232C>G
XM_011518626.1:c.4146C>G	XP_011516928.1:p.Ile1382Met
XM_011518627.1:c.3873C>G	XP_011516929.1:p.Ile1291Met
XM_011518628.1:c.3761-4232C>G	XP_011516930.1:n.3761-4232C>G
XM_011518629.1:c.3597C>G	XP_011516931.1:p.Ile1199Met
XM_005251972.4:c.4689C>G	XP_005252029.1:p.Ile1563Met
XM_005251973.4:c.4034-4232C>G	XP_005252030.1:n.4034-4232C>G
XM_005251974.4:c.3324C>G	XP_005252031.1:p.Ile1108Met
XM_005251975.4:c.3215-4232C>G	XP_005252032.1:n.3215-4232C>G
XM_006717096.4:c.5238C>G	XP_006717159.1:p.Ile1746Met
XM_006717097.4:c.4689C>G	XP_006717160.1:p.Ile1563Met
XM_006717098.4:c.4416C>G	XP_006717161.1:p.Ile1472Met
XM_006717101.4:c.3488-4232C>G	XP_006717164.1:n.3488-4232C>G
XM_011518625.3:c.4580-4232C>G	XP_011516927.1:n.4580-4232C>G
XM_011518626.3:c.4146C>G	XP_011516928.1:p.Ile1382Met
XM_011518628.3:c.3761-4232C>G	XP_011516930.1:n.3761-4232C>G
XM_011518629.3:c.3597C>G	XP_011516931.1:p.Ile1199Met
XM_017014678.2:c.5511C>G	XP_016870167.1:p.Ile1837Met
XM_017014679.2:c.5238C>G	XP_016870168.1:p.Ile1746Met
XM_017014680.2:c.5235C>G	XP_016870169.1:p.Ile1745Met
XM_017014681.2:c.4419C>G	XP_016870170.1:p.Ile1473Met
XM_024447530.1:c.5511C>G	XP_024303298.1:p.Ile1837Met
NM_002160.4:c.4962C>G MANE Select	NP_002151.2:p.Ile1654Met