Canonical Allele Identifier: CA374630875

Gene: TNC

Linked Data

• MyVariant Identifiers: chr9:g.117808786G>C (hg19) ; chr9:g.115046507G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115046507G>C , CM000671.2:g.115046507G>C	GRCh38
NC_000009.11:g.117808786G>C , CM000671.1:g.117808786G>C	GRCh37
NC_000009.10:g.116848607G>C	NCBI36
NG_029637.1:g.76751C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000476680.2:c.318-4166C>G
ENST00000537320.6:c.3215-4166C>G	ENSP00000443478.1:n.3215-4166C>G
ENST00000542877.6:c.3939C>G	ENSP00000442242.1:p.Asp1313Glu
ENST00000705190.1:c.1971C>G	ENSP00000516083.1:p.Asp657Glu
ENST00000705191.1:c.627C>G	ENSP00000516084.1:p.Asp209Glu
ENST00000705192.1:c.3986C>G
ENST00000350763.9:c.5028C>G MANE Select	ENSP00000265131.4:p.Asp1676Glu
ENST00000341037.8:c.4482C>G	ENSP00000339553.4:p.Asp1494Glu
ENST00000350763.8:c.5028C>G	ENSP00000265131.4:p.Asp1676Glu
ENST00000423613.6:c.4307-4166C>G	ENSP00000411406.2:n.4307-4166C>G
ENST00000473855.1:n.346C>G
ENST00000476680.1:n.253-4166C>G
ENST00000498724.5:n.40-4166C>G
ENST00000535648.5:c.3939C>G	ENSP00000438152.2:p.Asp1313Glu
ENST00000537320.5:c.3215-4166C>G	ENSP00000443478.1:n.3215-4166C>G
ENST00000542877.5:c.3939C>G	ENSP00000442242.1:p.Asp1313Glu
ENST00000544972.1:c.715C>G
NM_002160.3:c.5028C>G	NP_002151.2:p.Asp1676Glu
XM_005251972.2:c.4755C>G	XP_005252029.1:p.Asp1585Glu
XM_005251973.2:c.4034-4166C>G	XP_005252030.1:n.4034-4166C>G
XM_005251974.2:c.3390C>G	XP_005252031.1:p.Asp1130Glu
XM_005251975.2:c.3215-4166C>G	XP_005252032.1:n.3215-4166C>G
XM_006717096.2:c.5304C>G	XP_006717159.1:p.Asp1768Glu
XM_006717097.2:c.4755C>G	XP_006717160.1:p.Asp1585Glu
XM_006717098.2:c.4482C>G	XP_006717161.1:p.Asp1494Glu
XM_006717100.2:c.4307-4166C>G	XP_006717163.1:n.4307-4166C>G
XM_006717101.2:c.3488-4166C>G	XP_006717164.1:n.3488-4166C>G
XM_011518622.1:c.5031C>G	XP_011516924.1:p.Asp1677Glu
XM_011518623.1:c.5031C>G	XP_011516925.1:p.Asp1677Glu
XM_011518624.1:c.4485C>G	XP_011516926.1:p.Asp1495Glu
XM_011518625.1:c.4580-4166C>G	XP_011516927.1:n.4580-4166C>G
XM_011518626.1:c.4212C>G	XP_011516928.1:p.Asp1404Glu
XM_011518627.1:c.3939C>G	XP_011516929.1:p.Asp1313Glu
XM_011518628.1:c.3761-4166C>G	XP_011516930.1:n.3761-4166C>G
XM_011518629.1:c.3663C>G	XP_011516931.1:p.Asp1221Glu
XM_005251972.4:c.4755C>G	XP_005252029.1:p.Asp1585Glu
XM_005251973.4:c.4034-4166C>G	XP_005252030.1:n.4034-4166C>G
XM_005251974.4:c.3390C>G	XP_005252031.1:p.Asp1130Glu
XM_005251975.4:c.3215-4166C>G	XP_005252032.1:n.3215-4166C>G
XM_006717096.4:c.5304C>G	XP_006717159.1:p.Asp1768Glu
XM_006717097.4:c.4755C>G	XP_006717160.1:p.Asp1585Glu
XM_006717098.4:c.4482C>G	XP_006717161.1:p.Asp1494Glu
XM_006717101.4:c.3488-4166C>G	XP_006717164.1:n.3488-4166C>G
XM_011518625.3:c.4580-4166C>G	XP_011516927.1:n.4580-4166C>G
XM_011518626.3:c.4212C>G	XP_011516928.1:p.Asp1404Glu
XM_011518628.3:c.3761-4166C>G	XP_011516930.1:n.3761-4166C>G
XM_011518629.3:c.3663C>G	XP_011516931.1:p.Asp1221Glu
XM_017014678.2:c.5577C>G	XP_016870167.1:p.Asp1859Glu
XM_017014679.2:c.5304C>G	XP_016870168.1:p.Asp1768Glu
XM_017014680.2:c.5301C>G	XP_016870169.1:p.Asp1767Glu
XM_017014681.2:c.4485C>G	XP_016870170.1:p.Asp1495Glu
XM_024447530.1:c.5577C>G	XP_024303298.1:p.Asp1859Glu
NM_002160.4:c.5028C>G MANE Select	NP_002151.2:p.Asp1676Glu