Canonical Allele Identifier: CA374626441

Gene: TNC

Linked Data

• MyVariant Identifiers: chr9:g.117797506C>G (hg19) ; chr9:g.115035227C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035227C>G , CM000671.2:g.115035227C>G	GRCh38
NC_000009.11:g.117797506C>G , CM000671.1:g.117797506C>G	GRCh37
NC_000009.10:g.116837327C>G	NCBI36
NG_029637.1:g.88031G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000537320.6:c.3853G>C	ENSP00000443478.1:p.Glu1285Gln
ENST00000542877.6:c.4675G>C	ENSP00000442242.1:p.Glu1559Gln
ENST00000705190.1:c.2707G>C	ENSP00000516083.1:p.Glu903Gln
ENST00000705191.1:c.1363G>C	ENSP00000516084.1:p.Glu455Gln
ENST00000705192.1:c.4722G>C
ENST00000350763.9:c.5764G>C MANE Select	ENSP00000265131.4:p.Glu1922Gln
ENST00000341037.8:c.5218G>C	ENSP00000339553.4:p.Glu1740Gln
ENST00000350763.8:c.5764G>C	ENSP00000265131.4:p.Glu1922Gln
ENST00000423613.6:c.4945G>C	ENSP00000411406.2:p.Glu1649Gln
ENST00000460345.1:n.346G>C
ENST00000535648.5:c.4675G>C	ENSP00000438152.2:p.Glu1559Gln
ENST00000537320.5:c.3853G>C	ENSP00000443478.1:p.Glu1285Gln
ENST00000542877.5:c.4675G>C	ENSP00000442242.1:p.Glu1559Gln
ENST00000544972.1:c.1451G>C
NM_002160.3:c.5764G>C	NP_002151.2:p.Glu1922Gln
XM_005251972.2:c.5491G>C	XP_005252029.1:p.Glu1831Gln
XM_005251973.2:c.4672G>C	XP_005252030.1:p.Glu1558Gln
XM_005251974.2:c.4126G>C	XP_005252031.1:p.Glu1376Gln
XM_005251975.2:c.3853G>C	XP_005252032.1:p.Glu1285Gln
XM_006717096.2:c.6040G>C	XP_006717159.1:p.Glu2014Gln
XM_006717097.2:c.5491G>C	XP_006717160.1:p.Glu1831Gln
XM_006717098.2:c.5218G>C	XP_006717161.1:p.Glu1740Gln
XM_006717100.2:c.4945G>C	XP_006717163.1:p.Glu1649Gln
XM_006717101.2:c.4126G>C	XP_006717164.1:p.Glu1376Gln
XM_011518622.1:c.5767G>C	XP_011516924.1:p.Glu1923Gln
XM_011518623.1:c.5767G>C	XP_011516925.1:p.Glu1923Gln
XM_011518624.1:c.5221G>C	XP_011516926.1:p.Glu1741Gln
XM_011518625.1:c.5218G>C	XP_011516927.1:p.Glu1740Gln
XM_011518626.1:c.4948G>C	XP_011516928.1:p.Glu1650Gln
XM_011518627.1:c.4675G>C	XP_011516929.1:p.Glu1559Gln
XM_011518628.1:c.4399G>C	XP_011516930.1:p.Glu1467Gln
XM_011518629.1:c.4399G>C	XP_011516931.1:p.Glu1467Gln
XM_005251972.4:c.5491G>C	XP_005252029.1:p.Glu1831Gln
XM_005251973.4:c.4672G>C	XP_005252030.1:p.Glu1558Gln
XM_005251974.4:c.4126G>C	XP_005252031.1:p.Glu1376Gln
XM_005251975.4:c.3853G>C	XP_005252032.1:p.Glu1285Gln
XM_006717096.4:c.6040G>C	XP_006717159.1:p.Glu2014Gln
XM_006717097.4:c.5491G>C	XP_006717160.1:p.Glu1831Gln
XM_006717098.4:c.5218G>C	XP_006717161.1:p.Glu1740Gln
XM_006717101.4:c.4126G>C	XP_006717164.1:p.Glu1376Gln
XM_011518625.3:c.5218G>C	XP_011516927.1:p.Glu1740Gln
XM_011518626.3:c.4948G>C	XP_011516928.1:p.Glu1650Gln
XM_011518628.3:c.4399G>C	XP_011516930.1:p.Glu1467Gln
XM_011518629.3:c.4399G>C	XP_011516931.1:p.Glu1467Gln
XM_017014678.2:c.6313G>C	XP_016870167.1:p.Glu2105Gln
XM_017014679.2:c.6040G>C	XP_016870168.1:p.Glu2014Gln
XM_017014680.2:c.6037G>C	XP_016870169.1:p.Glu2013Gln
XM_017014681.2:c.5221G>C	XP_016870170.1:p.Glu1741Gln
XM_024447530.1:c.6313G>C	XP_024303298.1:p.Glu2105Gln
NM_002160.4:c.5764G>C MANE Select	NP_002151.2:p.Glu1922Gln