Canonical Allele Identifier: CA5207543

Gene: TNC

Linked Data

• ClinVar Variation Id: 2682303
• ClinVar RCV Id: RCV003479676
• dbSNP Id: rs747230674
• ExAC: 9:117797512 C / A
• gnomAD v2: 9-117797512-C-A
• gnomAD v3: 9-115035233-C-A
• gnomAD v4: 9-115035233-C-A
• MyVariant Identifiers: chr9:g.117797512C>A (hg19) ; chr9:g.115035233C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035233C>A , CM000671.2:g.115035233C>A	GRCh38
NC_000009.11:g.117797512C>A , CM000671.1:g.117797512C>A	GRCh37
NC_000009.10:g.116837333C>A	NCBI36
NG_029637.1:g.88025G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000537320.6:c.3847G>T	ENSP00000443478.1:p.Val1283Phe
ENST00000542877.6:c.4669G>T	ENSP00000442242.1:p.Val1557Phe
ENST00000705190.1:c.2701G>T	ENSP00000516083.1:p.Val901Phe
ENST00000705191.1:c.1357G>T	ENSP00000516084.1:p.Val453Phe
ENST00000705192.1:c.4716G>T
ENST00000350763.9:c.5758G>T MANE Select	ENSP00000265131.4:p.Val1920Phe
ENST00000341037.8:c.5212G>T	ENSP00000339553.4:p.Val1738Phe
ENST00000350763.8:c.5758G>T	ENSP00000265131.4:p.Val1920Phe
ENST00000423613.6:c.4939G>T	ENSP00000411406.2:p.Val1647Phe
ENST00000460345.1:n.340G>T
ENST00000535648.5:c.4669G>T	ENSP00000438152.2:p.Val1557Phe
ENST00000537320.5:c.3847G>T	ENSP00000443478.1:p.Val1283Phe
ENST00000542877.5:c.4669G>T	ENSP00000442242.1:p.Val1557Phe
ENST00000544972.1:c.1445G>T
NM_002160.3:c.5758G>T	NP_002151.2:p.Val1920Phe
XM_005251972.2:c.5485G>T	XP_005252029.1:p.Val1829Phe
XM_005251973.2:c.4666G>T	XP_005252030.1:p.Val1556Phe
XM_005251974.2:c.4120G>T	XP_005252031.1:p.Val1374Phe
XM_005251975.2:c.3847G>T	XP_005252032.1:p.Val1283Phe
XM_006717096.2:c.6034G>T	XP_006717159.1:p.Val2012Phe
XM_006717097.2:c.5485G>T	XP_006717160.1:p.Val1829Phe
XM_006717098.2:c.5212G>T	XP_006717161.1:p.Val1738Phe
XM_006717100.2:c.4939G>T	XP_006717163.1:p.Val1647Phe
XM_006717101.2:c.4120G>T	XP_006717164.1:p.Val1374Phe
XM_011518622.1:c.5761G>T	XP_011516924.1:p.Val1921Phe
XM_011518623.1:c.5761G>T	XP_011516925.1:p.Val1921Phe
XM_011518624.1:c.5215G>T	XP_011516926.1:p.Val1739Phe
XM_011518625.1:c.5212G>T	XP_011516927.1:p.Val1738Phe
XM_011518626.1:c.4942G>T	XP_011516928.1:p.Val1648Phe
XM_011518627.1:c.4669G>T	XP_011516929.1:p.Val1557Phe
XM_011518628.1:c.4393G>T	XP_011516930.1:p.Val1465Phe
XM_011518629.1:c.4393G>T	XP_011516931.1:p.Val1465Phe
XM_005251972.4:c.5485G>T	XP_005252029.1:p.Val1829Phe
XM_005251973.4:c.4666G>T	XP_005252030.1:p.Val1556Phe
XM_005251974.4:c.4120G>T	XP_005252031.1:p.Val1374Phe
XM_005251975.4:c.3847G>T	XP_005252032.1:p.Val1283Phe
XM_006717096.4:c.6034G>T	XP_006717159.1:p.Val2012Phe
XM_006717097.4:c.5485G>T	XP_006717160.1:p.Val1829Phe
XM_006717098.4:c.5212G>T	XP_006717161.1:p.Val1738Phe
XM_006717101.4:c.4120G>T	XP_006717164.1:p.Val1374Phe
XM_011518625.3:c.5212G>T	XP_011516927.1:p.Val1738Phe
XM_011518626.3:c.4942G>T	XP_011516928.1:p.Val1648Phe
XM_011518628.3:c.4393G>T	XP_011516930.1:p.Val1465Phe
XM_011518629.3:c.4393G>T	XP_011516931.1:p.Val1465Phe
XM_017014678.2:c.6307G>T	XP_016870167.1:p.Val2103Phe
XM_017014679.2:c.6034G>T	XP_016870168.1:p.Val2012Phe
XM_017014680.2:c.6031G>T	XP_016870169.1:p.Val2011Phe
XM_017014681.2:c.5215G>T	XP_016870170.1:p.Val1739Phe
XM_024447530.1:c.6307G>T	XP_024303298.1:p.Val2103Phe
NM_002160.4:c.5758G>T MANE Select	NP_002151.2:p.Val1920Phe