Canonical Allele Identifier: CA374626567

Gene: TNC

Linked Data

• MyVariant Identifiers: chr9:g.117797575G>A (hg19) ; chr9:g.115035296G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035296G>A , CM000671.2:g.115035296G>A	GRCh38
NC_000009.11:g.117797575G>A , CM000671.1:g.117797575G>A	GRCh37
NC_000009.10:g.116837396G>A	NCBI36
NG_029637.1:g.87962C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537320.6:c.3784C>T	ENSP00000443478.1:p.Gln1262Ter
ENST00000542877.6:c.4606C>T	ENSP00000442242.1:p.Gln1536Ter
ENST00000705190.1:c.2638C>T	ENSP00000516083.1:p.Gln880Ter
ENST00000705191.1:c.1294C>T	ENSP00000516084.1:p.Gln432Ter
ENST00000705192.1:c.4653C>T
ENST00000350763.9:c.5695C>T MANE Select	ENSP00000265131.4:p.Gln1899Ter
ENST00000341037.8:c.5149C>T	ENSP00000339553.4:p.Gln1717Ter
ENST00000350763.8:c.5695C>T	ENSP00000265131.4:p.Gln1899Ter
ENST00000423613.6:c.4876C>T	ENSP00000411406.2:p.Gln1626Ter
ENST00000460345.1:n.277C>T
ENST00000535648.5:c.4606C>T	ENSP00000438152.2:p.Gln1536Ter
ENST00000537320.5:c.3784C>T	ENSP00000443478.1:p.Gln1262Ter
ENST00000542877.5:c.4606C>T	ENSP00000442242.1:p.Gln1536Ter
ENST00000544972.1:c.1382C>T
NM_002160.3:c.5695C>T	NP_002151.2:p.Gln1899Ter
XM_005251972.2:c.5422C>T	XP_005252029.1:p.Gln1808Ter
XM_005251973.2:c.4603C>T	XP_005252030.1:p.Gln1535Ter
XM_005251974.2:c.4057C>T	XP_005252031.1:p.Gln1353Ter
XM_005251975.2:c.3784C>T	XP_005252032.1:p.Gln1262Ter
XM_006717096.2:c.5971C>T	XP_006717159.1:p.Gln1991Ter
XM_006717097.2:c.5422C>T	XP_006717160.1:p.Gln1808Ter
XM_006717098.2:c.5149C>T	XP_006717161.1:p.Gln1717Ter
XM_006717100.2:c.4876C>T	XP_006717163.1:p.Gln1626Ter
XM_006717101.2:c.4057C>T	XP_006717164.1:p.Gln1353Ter
XM_011518622.1:c.5698C>T	XP_011516924.1:p.Gln1900Ter
XM_011518623.1:c.5698C>T	XP_011516925.1:p.Gln1900Ter
XM_011518624.1:c.5152C>T	XP_011516926.1:p.Gln1718Ter
XM_011518625.1:c.5149C>T	XP_011516927.1:p.Gln1717Ter
XM_011518626.1:c.4879C>T	XP_011516928.1:p.Gln1627Ter
XM_011518627.1:c.4606C>T	XP_011516929.1:p.Gln1536Ter
XM_011518628.1:c.4330C>T	XP_011516930.1:p.Gln1444Ter
XM_011518629.1:c.4330C>T	XP_011516931.1:p.Gln1444Ter
XM_005251972.4:c.5422C>T	XP_005252029.1:p.Gln1808Ter
XM_005251973.4:c.4603C>T	XP_005252030.1:p.Gln1535Ter
XM_005251974.4:c.4057C>T	XP_005252031.1:p.Gln1353Ter
XM_005251975.4:c.3784C>T	XP_005252032.1:p.Gln1262Ter
XM_006717096.4:c.5971C>T	XP_006717159.1:p.Gln1991Ter
XM_006717097.4:c.5422C>T	XP_006717160.1:p.Gln1808Ter
XM_006717098.4:c.5149C>T	XP_006717161.1:p.Gln1717Ter
XM_006717101.4:c.4057C>T	XP_006717164.1:p.Gln1353Ter
XM_011518625.3:c.5149C>T	XP_011516927.1:p.Gln1717Ter
XM_011518626.3:c.4879C>T	XP_011516928.1:p.Gln1627Ter
XM_011518628.3:c.4330C>T	XP_011516930.1:p.Gln1444Ter
XM_011518629.3:c.4330C>T	XP_011516931.1:p.Gln1444Ter
XM_017014678.2:c.6244C>T	XP_016870167.1:p.Gln2082Ter
XM_017014679.2:c.5971C>T	XP_016870168.1:p.Gln1991Ter
XM_017014680.2:c.5968C>T	XP_016870169.1:p.Gln1990Ter
XM_017014681.2:c.5152C>T	XP_016870170.1:p.Gln1718Ter
XM_024447530.1:c.6244C>T	XP_024303298.1:p.Gln2082Ter
NM_002160.4:c.5695C>T MANE Select	NP_002151.2:p.Gln1899Ter