Canonical Allele Identifier: CA466790299

Gene: TNC

Linked Data

• dbSNP Id: rs1379227314
• MyVariant Identifiers: chr9:g.117797579C>T (hg19) ; chr9:g.115035300C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035300C>T , CM000671.2:g.115035300C>T	GRCh38
NC_000009.11:g.117797579C>T , CM000671.1:g.117797579C>T	GRCh37
NC_000009.10:g.116837400C>T	NCBI36
NG_029637.1:g.87958G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537320.6:c.3780G>A	ENSP00000443478.1:p.Glu1260=
ENST00000542877.6:c.4602G>A	ENSP00000442242.1:p.Glu1534=
ENST00000705190.1:c.2634G>A	ENSP00000516083.1:p.Glu878=
ENST00000705191.1:c.1290G>A	ENSP00000516084.1:p.Glu430=
ENST00000705192.1:c.4649G>A
ENST00000350763.9:c.5691G>A MANE Select	ENSP00000265131.4:p.Glu1897=
ENST00000341037.8:c.5145G>A	ENSP00000339553.4:p.Glu1715=
ENST00000350763.8:c.5691G>A	ENSP00000265131.4:p.Glu1897=
ENST00000423613.6:c.4872G>A	ENSP00000411406.2:p.Glu1624=
ENST00000460345.1:n.273G>A
ENST00000535648.5:c.4602G>A	ENSP00000438152.2:p.Glu1534=
ENST00000537320.5:c.3780G>A	ENSP00000443478.1:p.Glu1260=
ENST00000542877.5:c.4602G>A	ENSP00000442242.1:p.Glu1534=
ENST00000544972.1:c.1378G>A
NM_002160.3:c.5691G>A	NP_002151.2:p.Glu1897=
XM_005251972.2:c.5418G>A	XP_005252029.1:p.Glu1806=
XM_005251973.2:c.4599G>A	XP_005252030.1:p.Glu1533=
XM_005251974.2:c.4053G>A	XP_005252031.1:p.Glu1351=
XM_005251975.2:c.3780G>A	XP_005252032.1:p.Glu1260=
XM_006717096.2:c.5967G>A	XP_006717159.1:p.Glu1989=
XM_006717097.2:c.5418G>A	XP_006717160.1:p.Glu1806=
XM_006717098.2:c.5145G>A	XP_006717161.1:p.Glu1715=
XM_006717100.2:c.4872G>A	XP_006717163.1:p.Glu1624=
XM_006717101.2:c.4053G>A	XP_006717164.1:p.Glu1351=
XM_011518622.1:c.5694G>A	XP_011516924.1:p.Glu1898=
XM_011518623.1:c.5694G>A	XP_011516925.1:p.Glu1898=
XM_011518624.1:c.5148G>A	XP_011516926.1:p.Glu1716=
XM_011518625.1:c.5145G>A	XP_011516927.1:p.Glu1715=
XM_011518626.1:c.4875G>A	XP_011516928.1:p.Glu1625=
XM_011518627.1:c.4602G>A	XP_011516929.1:p.Glu1534=
XM_011518628.1:c.4326G>A	XP_011516930.1:p.Glu1442=
XM_011518629.1:c.4326G>A	XP_011516931.1:p.Glu1442=
XM_005251972.4:c.5418G>A	XP_005252029.1:p.Glu1806=
XM_005251973.4:c.4599G>A	XP_005252030.1:p.Glu1533=
XM_005251974.4:c.4053G>A	XP_005252031.1:p.Glu1351=
XM_005251975.4:c.3780G>A	XP_005252032.1:p.Glu1260=
XM_006717096.4:c.5967G>A	XP_006717159.1:p.Glu1989=
XM_006717097.4:c.5418G>A	XP_006717160.1:p.Glu1806=
XM_006717098.4:c.5145G>A	XP_006717161.1:p.Glu1715=
XM_006717101.4:c.4053G>A	XP_006717164.1:p.Glu1351=
XM_011518625.3:c.5145G>A	XP_011516927.1:p.Glu1715=
XM_011518626.3:c.4875G>A	XP_011516928.1:p.Glu1625=
XM_011518628.3:c.4326G>A	XP_011516930.1:p.Glu1442=
XM_011518629.3:c.4326G>A	XP_011516931.1:p.Glu1442=
XM_017014678.2:c.6240G>A	XP_016870167.1:p.Glu2080=
XM_017014679.2:c.5967G>A	XP_016870168.1:p.Glu1989=
XM_017014680.2:c.5964G>A	XP_016870169.1:p.Glu1988=
XM_017014681.2:c.5148G>A	XP_016870170.1:p.Glu1716=
XM_024447530.1:c.6240G>A	XP_024303298.1:p.Glu2080=
NM_002160.4:c.5691G>A MANE Select	NP_002151.2:p.Glu1897=