Canonical Allele Identifier: CA374626553

Gene: TNC

Linked Data

• MyVariant Identifiers: chr9:g.117797567T>G (hg19) ; chr9:g.115035288T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035288T>G , CM000671.2:g.115035288T>G	GRCh38
NC_000009.11:g.117797567T>G , CM000671.1:g.117797567T>G	GRCh37
NC_000009.10:g.116837388T>G	NCBI36
NG_029637.1:g.87970A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537320.6:c.3792A>C	ENSP00000443478.1:p.Glu1264Asp
ENST00000542877.6:c.4614A>C	ENSP00000442242.1:p.Glu1538Asp
ENST00000705190.1:c.2646A>C	ENSP00000516083.1:p.Glu882Asp
ENST00000705191.1:c.1302A>C	ENSP00000516084.1:p.Glu434Asp
ENST00000705192.1:c.4661A>C
ENST00000350763.9:c.5703A>C MANE Select	ENSP00000265131.4:p.Glu1901Asp
ENST00000341037.8:c.5157A>C	ENSP00000339553.4:p.Glu1719Asp
ENST00000350763.8:c.5703A>C	ENSP00000265131.4:p.Glu1901Asp
ENST00000423613.6:c.4884A>C	ENSP00000411406.2:p.Glu1628Asp
ENST00000460345.1:n.285A>C
ENST00000535648.5:c.4614A>C	ENSP00000438152.2:p.Glu1538Asp
ENST00000537320.5:c.3792A>C	ENSP00000443478.1:p.Glu1264Asp
ENST00000542877.5:c.4614A>C	ENSP00000442242.1:p.Glu1538Asp
ENST00000544972.1:c.1390A>C
NM_002160.3:c.5703A>C	NP_002151.2:p.Glu1901Asp
XM_005251972.2:c.5430A>C	XP_005252029.1:p.Glu1810Asp
XM_005251973.2:c.4611A>C	XP_005252030.1:p.Glu1537Asp
XM_005251974.2:c.4065A>C	XP_005252031.1:p.Glu1355Asp
XM_005251975.2:c.3792A>C	XP_005252032.1:p.Glu1264Asp
XM_006717096.2:c.5979A>C	XP_006717159.1:p.Glu1993Asp
XM_006717097.2:c.5430A>C	XP_006717160.1:p.Glu1810Asp
XM_006717098.2:c.5157A>C	XP_006717161.1:p.Glu1719Asp
XM_006717100.2:c.4884A>C	XP_006717163.1:p.Glu1628Asp
XM_006717101.2:c.4065A>C	XP_006717164.1:p.Glu1355Asp
XM_011518622.1:c.5706A>C	XP_011516924.1:p.Glu1902Asp
XM_011518623.1:c.5706A>C	XP_011516925.1:p.Glu1902Asp
XM_011518624.1:c.5160A>C	XP_011516926.1:p.Glu1720Asp
XM_011518625.1:c.5157A>C	XP_011516927.1:p.Glu1719Asp
XM_011518626.1:c.4887A>C	XP_011516928.1:p.Glu1629Asp
XM_011518627.1:c.4614A>C	XP_011516929.1:p.Glu1538Asp
XM_011518628.1:c.4338A>C	XP_011516930.1:p.Glu1446Asp
XM_011518629.1:c.4338A>C	XP_011516931.1:p.Glu1446Asp
XM_005251972.4:c.5430A>C	XP_005252029.1:p.Glu1810Asp
XM_005251973.4:c.4611A>C	XP_005252030.1:p.Glu1537Asp
XM_005251974.4:c.4065A>C	XP_005252031.1:p.Glu1355Asp
XM_005251975.4:c.3792A>C	XP_005252032.1:p.Glu1264Asp
XM_006717096.4:c.5979A>C	XP_006717159.1:p.Glu1993Asp
XM_006717097.4:c.5430A>C	XP_006717160.1:p.Glu1810Asp
XM_006717098.4:c.5157A>C	XP_006717161.1:p.Glu1719Asp
XM_006717101.4:c.4065A>C	XP_006717164.1:p.Glu1355Asp
XM_011518625.3:c.5157A>C	XP_011516927.1:p.Glu1719Asp
XM_011518626.3:c.4887A>C	XP_011516928.1:p.Glu1629Asp
XM_011518628.3:c.4338A>C	XP_011516930.1:p.Glu1446Asp
XM_011518629.3:c.4338A>C	XP_011516931.1:p.Glu1446Asp
XM_017014678.2:c.6252A>C	XP_016870167.1:p.Glu2084Asp
XM_017014679.2:c.5979A>C	XP_016870168.1:p.Glu1993Asp
XM_017014680.2:c.5976A>C	XP_016870169.1:p.Glu1992Asp
XM_017014681.2:c.5160A>C	XP_016870170.1:p.Glu1720Asp
XM_024447530.1:c.6252A>C	XP_024303298.1:p.Glu2084Asp
NM_002160.4:c.5703A>C MANE Select	NP_002151.2:p.Glu1901Asp