Canonical Allele Identifier: CA374626487

Gene: TNC

Linked Data

• MyVariant Identifiers: chr9:g.117797530C>A (hg19) ; chr9:g.115035251C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035251C>A , CM000671.2:g.115035251C>A	GRCh38
NC_000009.11:g.117797530C>A , CM000671.1:g.117797530C>A	GRCh37
NC_000009.10:g.116837351C>A	NCBI36
NG_029637.1:g.88007G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537320.6:c.3829G>T	ENSP00000443478.1:p.Val1277Phe
ENST00000542877.6:c.4651G>T	ENSP00000442242.1:p.Val1551Phe
ENST00000705190.1:c.2683G>T	ENSP00000516083.1:p.Val895Phe
ENST00000705191.1:c.1339G>T	ENSP00000516084.1:p.Val447Phe
ENST00000705192.1:c.4698G>T
ENST00000350763.9:c.5740G>T MANE Select	ENSP00000265131.4:p.Val1914Phe
ENST00000341037.8:c.5194G>T	ENSP00000339553.4:p.Val1732Phe
ENST00000350763.8:c.5740G>T	ENSP00000265131.4:p.Val1914Phe
ENST00000423613.6:c.4921G>T	ENSP00000411406.2:p.Val1641Phe
ENST00000460345.1:n.322G>T
ENST00000535648.5:c.4651G>T	ENSP00000438152.2:p.Val1551Phe
ENST00000537320.5:c.3829G>T	ENSP00000443478.1:p.Val1277Phe
ENST00000542877.5:c.4651G>T	ENSP00000442242.1:p.Val1551Phe
ENST00000544972.1:c.1427G>T
NM_002160.3:c.5740G>T	NP_002151.2:p.Val1914Phe
XM_005251972.2:c.5467G>T	XP_005252029.1:p.Val1823Phe
XM_005251973.2:c.4648G>T	XP_005252030.1:p.Val1550Phe
XM_005251974.2:c.4102G>T	XP_005252031.1:p.Val1368Phe
XM_005251975.2:c.3829G>T	XP_005252032.1:p.Val1277Phe
XM_006717096.2:c.6016G>T	XP_006717159.1:p.Val2006Phe
XM_006717097.2:c.5467G>T	XP_006717160.1:p.Val1823Phe
XM_006717098.2:c.5194G>T	XP_006717161.1:p.Val1732Phe
XM_006717100.2:c.4921G>T	XP_006717163.1:p.Val1641Phe
XM_006717101.2:c.4102G>T	XP_006717164.1:p.Val1368Phe
XM_011518622.1:c.5743G>T	XP_011516924.1:p.Val1915Phe
XM_011518623.1:c.5743G>T	XP_011516925.1:p.Val1915Phe
XM_011518624.1:c.5197G>T	XP_011516926.1:p.Val1733Phe
XM_011518625.1:c.5194G>T	XP_011516927.1:p.Val1732Phe
XM_011518626.1:c.4924G>T	XP_011516928.1:p.Val1642Phe
XM_011518627.1:c.4651G>T	XP_011516929.1:p.Val1551Phe
XM_011518628.1:c.4375G>T	XP_011516930.1:p.Val1459Phe
XM_011518629.1:c.4375G>T	XP_011516931.1:p.Val1459Phe
XM_005251972.4:c.5467G>T	XP_005252029.1:p.Val1823Phe
XM_005251973.4:c.4648G>T	XP_005252030.1:p.Val1550Phe
XM_005251974.4:c.4102G>T	XP_005252031.1:p.Val1368Phe
XM_005251975.4:c.3829G>T	XP_005252032.1:p.Val1277Phe
XM_006717096.4:c.6016G>T	XP_006717159.1:p.Val2006Phe
XM_006717097.4:c.5467G>T	XP_006717160.1:p.Val1823Phe
XM_006717098.4:c.5194G>T	XP_006717161.1:p.Val1732Phe
XM_006717101.4:c.4102G>T	XP_006717164.1:p.Val1368Phe
XM_011518625.3:c.5194G>T	XP_011516927.1:p.Val1732Phe
XM_011518626.3:c.4924G>T	XP_011516928.1:p.Val1642Phe
XM_011518628.3:c.4375G>T	XP_011516930.1:p.Val1459Phe
XM_011518629.3:c.4375G>T	XP_011516931.1:p.Val1459Phe
XM_017014678.2:c.6289G>T	XP_016870167.1:p.Val2097Phe
XM_017014679.2:c.6016G>T	XP_016870168.1:p.Val2006Phe
XM_017014680.2:c.6013G>T	XP_016870169.1:p.Val2005Phe
XM_017014681.2:c.5197G>T	XP_016870170.1:p.Val1733Phe
XM_024447530.1:c.6289G>T	XP_024303298.1:p.Val2097Phe
NM_002160.4:c.5740G>T MANE Select	NP_002151.2:p.Val1914Phe