Canonical Allele Identifier: CA374631256

Gene: TNC

Linked Data

• MyVariant Identifiers: chr9:g.117808890C>A (hg19) ; chr9:g.115046611C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115046611C>A , CM000671.2:g.115046611C>A	GRCh38
NC_000009.11:g.117808890C>A , CM000671.1:g.117808890C>A	GRCh37
NC_000009.10:g.116848711C>A	NCBI36
NG_029637.1:g.76647G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476680.2:c.318-4270G>T
ENST00000537320.6:c.3215-4270G>T	ENSP00000443478.1:n.3215-4270G>T
ENST00000542877.6:c.3835G>T	ENSP00000442242.1:p.Ala1279Ser
ENST00000705190.1:c.1867G>T	ENSP00000516083.1:p.Ala623Ser
ENST00000705191.1:c.523G>T	ENSP00000516084.1:p.Ala175Ser
ENST00000705192.1:c.3882G>T
ENST00000350763.9:c.4924G>T MANE Select	ENSP00000265131.4:p.Ala1642Ser
ENST00000341037.8:c.4378G>T	ENSP00000339553.4:p.Ala1460Ser
ENST00000350763.8:c.4924G>T	ENSP00000265131.4:p.Ala1642Ser
ENST00000423613.6:c.4307-4270G>T	ENSP00000411406.2:n.4307-4270G>T
ENST00000473855.1:n.242G>T
ENST00000476680.1:n.253-4270G>T
ENST00000498724.5:n.40-4270G>T
ENST00000535648.5:c.3835G>T	ENSP00000438152.2:p.Ala1279Ser
ENST00000537320.5:c.3215-4270G>T	ENSP00000443478.1:n.3215-4270G>T
ENST00000542877.5:c.3835G>T	ENSP00000442242.1:p.Ala1279Ser
ENST00000544972.1:c.611G>T
NM_002160.3:c.4924G>T	NP_002151.2:p.Ala1642Ser
XM_005251972.2:c.4651G>T	XP_005252029.1:p.Ala1551Ser
XM_005251973.2:c.4034-4270G>T	XP_005252030.1:n.4034-4270G>T
XM_005251974.2:c.3286G>T	XP_005252031.1:p.Ala1096Ser
XM_005251975.2:c.3215-4270G>T	XP_005252032.1:n.3215-4270G>T
XM_006717096.2:c.5200G>T	XP_006717159.1:p.Ala1734Ser
XM_006717097.2:c.4651G>T	XP_006717160.1:p.Ala1551Ser
XM_006717098.2:c.4378G>T	XP_006717161.1:p.Ala1460Ser
XM_006717100.2:c.4307-4270G>T	XP_006717163.1:n.4307-4270G>T
XM_006717101.2:c.3488-4270G>T	XP_006717164.1:n.3488-4270G>T
XM_011518622.1:c.4927G>T	XP_011516924.1:p.Ala1643Ser
XM_011518623.1:c.4927G>T	XP_011516925.1:p.Ala1643Ser
XM_011518624.1:c.4381G>T	XP_011516926.1:p.Ala1461Ser
XM_011518625.1:c.4580-4270G>T	XP_011516927.1:n.4580-4270G>T
XM_011518626.1:c.4108G>T	XP_011516928.1:p.Ala1370Ser
XM_011518627.1:c.3835G>T	XP_011516929.1:p.Ala1279Ser
XM_011518628.1:c.3761-4270G>T	XP_011516930.1:n.3761-4270G>T
XM_011518629.1:c.3559G>T	XP_011516931.1:p.Ala1187Ser
XM_005251972.4:c.4651G>T	XP_005252029.1:p.Ala1551Ser
XM_005251973.4:c.4034-4270G>T	XP_005252030.1:n.4034-4270G>T
XM_005251974.4:c.3286G>T	XP_005252031.1:p.Ala1096Ser
XM_005251975.4:c.3215-4270G>T	XP_005252032.1:n.3215-4270G>T
XM_006717096.4:c.5200G>T	XP_006717159.1:p.Ala1734Ser
XM_006717097.4:c.4651G>T	XP_006717160.1:p.Ala1551Ser
XM_006717098.4:c.4378G>T	XP_006717161.1:p.Ala1460Ser
XM_006717101.4:c.3488-4270G>T	XP_006717164.1:n.3488-4270G>T
XM_011518625.3:c.4580-4270G>T	XP_011516927.1:n.4580-4270G>T
XM_011518626.3:c.4108G>T	XP_011516928.1:p.Ala1370Ser
XM_011518628.3:c.3761-4270G>T	XP_011516930.1:n.3761-4270G>T
XM_011518629.3:c.3559G>T	XP_011516931.1:p.Ala1187Ser
XM_017014678.2:c.5473G>T	XP_016870167.1:p.Ala1825Ser
XM_017014679.2:c.5200G>T	XP_016870168.1:p.Ala1734Ser
XM_017014680.2:c.5197G>T	XP_016870169.1:p.Ala1733Ser
XM_017014681.2:c.4381G>T	XP_016870170.1:p.Ala1461Ser
XM_024447530.1:c.5473G>T	XP_024303298.1:p.Ala1825Ser
NM_002160.4:c.4924G>T MANE Select	NP_002151.2:p.Ala1642Ser