Canonical Allele Identifier: CA374626439

Gene: TNC

Linked Data

• MyVariant Identifiers: chr9:g.117797505T>G (hg19) ; chr9:g.115035226T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035226T>G , CM000671.2:g.115035226T>G	GRCh38
NC_000009.11:g.117797505T>G , CM000671.1:g.117797505T>G	GRCh37
NC_000009.10:g.116837326T>G	NCBI36
NG_029637.1:g.88032A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000537320.6:c.3854A>C	ENSP00000443478.1:p.Glu1285Ala
ENST00000542877.6:c.4676A>C	ENSP00000442242.1:p.Glu1559Ala
ENST00000705190.1:c.2708A>C	ENSP00000516083.1:p.Glu903Ala
ENST00000705191.1:c.1364A>C	ENSP00000516084.1:p.Glu455Ala
ENST00000705192.1:c.4723A>C
ENST00000350763.9:c.5765A>C MANE Select	ENSP00000265131.4:p.Glu1922Ala
ENST00000341037.8:c.5219A>C	ENSP00000339553.4:p.Glu1740Ala
ENST00000350763.8:c.5765A>C	ENSP00000265131.4:p.Glu1922Ala
ENST00000423613.6:c.4946A>C	ENSP00000411406.2:p.Glu1649Ala
ENST00000460345.1:n.347A>C
ENST00000535648.5:c.4676A>C	ENSP00000438152.2:p.Glu1559Ala
ENST00000537320.5:c.3854A>C	ENSP00000443478.1:p.Glu1285Ala
ENST00000542877.5:c.4676A>C	ENSP00000442242.1:p.Glu1559Ala
ENST00000544972.1:c.1452A>C
NM_002160.3:c.5765A>C	NP_002151.2:p.Glu1922Ala
XM_005251972.2:c.5492A>C	XP_005252029.1:p.Glu1831Ala
XM_005251973.2:c.4673A>C	XP_005252030.1:p.Glu1558Ala
XM_005251974.2:c.4127A>C	XP_005252031.1:p.Glu1376Ala
XM_005251975.2:c.3854A>C	XP_005252032.1:p.Glu1285Ala
XM_006717096.2:c.6041A>C	XP_006717159.1:p.Glu2014Ala
XM_006717097.2:c.5492A>C	XP_006717160.1:p.Glu1831Ala
XM_006717098.2:c.5219A>C	XP_006717161.1:p.Glu1740Ala
XM_006717100.2:c.4946A>C	XP_006717163.1:p.Glu1649Ala
XM_006717101.2:c.4127A>C	XP_006717164.1:p.Glu1376Ala
XM_011518622.1:c.5768A>C	XP_011516924.1:p.Glu1923Ala
XM_011518623.1:c.5768A>C	XP_011516925.1:p.Glu1923Ala
XM_011518624.1:c.5222A>C	XP_011516926.1:p.Glu1741Ala
XM_011518625.1:c.5219A>C	XP_011516927.1:p.Glu1740Ala
XM_011518626.1:c.4949A>C	XP_011516928.1:p.Glu1650Ala
XM_011518627.1:c.4676A>C	XP_011516929.1:p.Glu1559Ala
XM_011518628.1:c.4400A>C	XP_011516930.1:p.Glu1467Ala
XM_011518629.1:c.4400A>C	XP_011516931.1:p.Glu1467Ala
XM_005251972.4:c.5492A>C	XP_005252029.1:p.Glu1831Ala
XM_005251973.4:c.4673A>C	XP_005252030.1:p.Glu1558Ala
XM_005251974.4:c.4127A>C	XP_005252031.1:p.Glu1376Ala
XM_005251975.4:c.3854A>C	XP_005252032.1:p.Glu1285Ala
XM_006717096.4:c.6041A>C	XP_006717159.1:p.Glu2014Ala
XM_006717097.4:c.5492A>C	XP_006717160.1:p.Glu1831Ala
XM_006717098.4:c.5219A>C	XP_006717161.1:p.Glu1740Ala
XM_006717101.4:c.4127A>C	XP_006717164.1:p.Glu1376Ala
XM_011518625.3:c.5219A>C	XP_011516927.1:p.Glu1740Ala
XM_011518626.3:c.4949A>C	XP_011516928.1:p.Glu1650Ala
XM_011518628.3:c.4400A>C	XP_011516930.1:p.Glu1467Ala
XM_011518629.3:c.4400A>C	XP_011516931.1:p.Glu1467Ala
XM_017014678.2:c.6314A>C	XP_016870167.1:p.Glu2105Ala
XM_017014679.2:c.6041A>C	XP_016870168.1:p.Glu2014Ala
XM_017014680.2:c.6038A>C	XP_016870169.1:p.Glu2013Ala
XM_017014681.2:c.5222A>C	XP_016870170.1:p.Glu1741Ala
XM_024447530.1:c.6314A>C	XP_024303298.1:p.Glu2105Ala
NM_002160.4:c.5765A>C MANE Select	NP_002151.2:p.Glu1922Ala