Canonical Allele Identifier: CA374626447

Gene: TNC

Linked Data

• MyVariant Identifiers: chr9:g.117797509A>C (hg19) ; chr9:g.115035230A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035230A>C , CM000671.2:g.115035230A>C	GRCh38
NC_000009.11:g.117797509A>C , CM000671.1:g.117797509A>C	GRCh37
NC_000009.10:g.116837330A>C	NCBI36
NG_029637.1:g.88028T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000537320.6:c.3850T>G	ENSP00000443478.1:p.Tyr1284Asp
ENST00000542877.6:c.4672T>G	ENSP00000442242.1:p.Tyr1558Asp
ENST00000705190.1:c.2704T>G	ENSP00000516083.1:p.Tyr902Asp
ENST00000705191.1:c.1360T>G	ENSP00000516084.1:p.Tyr454Asp
ENST00000705192.1:c.4719T>G
ENST00000350763.9:c.5761T>G MANE Select	ENSP00000265131.4:p.Tyr1921Asp
ENST00000341037.8:c.5215T>G	ENSP00000339553.4:p.Tyr1739Asp
ENST00000350763.8:c.5761T>G	ENSP00000265131.4:p.Tyr1921Asp
ENST00000423613.6:c.4942T>G	ENSP00000411406.2:p.Tyr1648Asp
ENST00000460345.1:n.343T>G
ENST00000535648.5:c.4672T>G	ENSP00000438152.2:p.Tyr1558Asp
ENST00000537320.5:c.3850T>G	ENSP00000443478.1:p.Tyr1284Asp
ENST00000542877.5:c.4672T>G	ENSP00000442242.1:p.Tyr1558Asp
ENST00000544972.1:c.1448T>G
NM_002160.3:c.5761T>G	NP_002151.2:p.Tyr1921Asp
XM_005251972.2:c.5488T>G	XP_005252029.1:p.Tyr1830Asp
XM_005251973.2:c.4669T>G	XP_005252030.1:p.Tyr1557Asp
XM_005251974.2:c.4123T>G	XP_005252031.1:p.Tyr1375Asp
XM_005251975.2:c.3850T>G	XP_005252032.1:p.Tyr1284Asp
XM_006717096.2:c.6037T>G	XP_006717159.1:p.Tyr2013Asp
XM_006717097.2:c.5488T>G	XP_006717160.1:p.Tyr1830Asp
XM_006717098.2:c.5215T>G	XP_006717161.1:p.Tyr1739Asp
XM_006717100.2:c.4942T>G	XP_006717163.1:p.Tyr1648Asp
XM_006717101.2:c.4123T>G	XP_006717164.1:p.Tyr1375Asp
XM_011518622.1:c.5764T>G	XP_011516924.1:p.Tyr1922Asp
XM_011518623.1:c.5764T>G	XP_011516925.1:p.Tyr1922Asp
XM_011518624.1:c.5218T>G	XP_011516926.1:p.Tyr1740Asp
XM_011518625.1:c.5215T>G	XP_011516927.1:p.Tyr1739Asp
XM_011518626.1:c.4945T>G	XP_011516928.1:p.Tyr1649Asp
XM_011518627.1:c.4672T>G	XP_011516929.1:p.Tyr1558Asp
XM_011518628.1:c.4396T>G	XP_011516930.1:p.Tyr1466Asp
XM_011518629.1:c.4396T>G	XP_011516931.1:p.Tyr1466Asp
XM_005251972.4:c.5488T>G	XP_005252029.1:p.Tyr1830Asp
XM_005251973.4:c.4669T>G	XP_005252030.1:p.Tyr1557Asp
XM_005251974.4:c.4123T>G	XP_005252031.1:p.Tyr1375Asp
XM_005251975.4:c.3850T>G	XP_005252032.1:p.Tyr1284Asp
XM_006717096.4:c.6037T>G	XP_006717159.1:p.Tyr2013Asp
XM_006717097.4:c.5488T>G	XP_006717160.1:p.Tyr1830Asp
XM_006717098.4:c.5215T>G	XP_006717161.1:p.Tyr1739Asp
XM_006717101.4:c.4123T>G	XP_006717164.1:p.Tyr1375Asp
XM_011518625.3:c.5215T>G	XP_011516927.1:p.Tyr1739Asp
XM_011518626.3:c.4945T>G	XP_011516928.1:p.Tyr1649Asp
XM_011518628.3:c.4396T>G	XP_011516930.1:p.Tyr1466Asp
XM_011518629.3:c.4396T>G	XP_011516931.1:p.Tyr1466Asp
XM_017014678.2:c.6310T>G	XP_016870167.1:p.Tyr2104Asp
XM_017014679.2:c.6037T>G	XP_016870168.1:p.Tyr2013Asp
XM_017014680.2:c.6034T>G	XP_016870169.1:p.Tyr2012Asp
XM_017014681.2:c.5218T>G	XP_016870170.1:p.Tyr1740Asp
XM_024447530.1:c.6310T>G	XP_024303298.1:p.Tyr2104Asp
NM_002160.4:c.5761T>G MANE Select	NP_002151.2:p.Tyr1921Asp