Canonical Allele Identifier: CA5207775

Gene: TNC

Linked Data

• dbSNP Id: rs757588594
• ExAC: 9:117808827 G / T
• gnomAD v2: 9-117808827-G-T
• gnomAD v4: 9-115046548-G-T
• MyVariant Identifiers: chr9:g.117808827G>T (hg19) ; chr9:g.115046548G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115046548G>T , CM000671.2:g.115046548G>T	GRCh38
NC_000009.11:g.117808827G>T , CM000671.1:g.117808827G>T	GRCh37
NC_000009.10:g.116848648G>T	NCBI36
NG_029637.1:g.76710C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476680.2:c.318-4207C>A
ENST00000537320.6:c.3215-4207C>A	ENSP00000443478.1:n.3215-4207C>A
ENST00000542877.6:c.3898C>A	ENSP00000442242.1:p.Pro1300Thr
ENST00000705190.1:c.1930C>A	ENSP00000516083.1:p.Pro644Thr
ENST00000705191.1:c.586C>A	ENSP00000516084.1:p.Pro196Thr
ENST00000705192.1:c.3945C>A
ENST00000350763.9:c.4987C>A MANE Select	ENSP00000265131.4:p.Pro1663Thr
ENST00000341037.8:c.4441C>A	ENSP00000339553.4:p.Pro1481Thr
ENST00000350763.8:c.4987C>A	ENSP00000265131.4:p.Pro1663Thr
ENST00000423613.6:c.4307-4207C>A	ENSP00000411406.2:n.4307-4207C>A
ENST00000473855.1:n.305C>A
ENST00000476680.1:n.253-4207C>A
ENST00000498724.5:n.40-4207C>A
ENST00000535648.5:c.3898C>A	ENSP00000438152.2:p.Pro1300Thr
ENST00000537320.5:c.3215-4207C>A	ENSP00000443478.1:n.3215-4207C>A
ENST00000542877.5:c.3898C>A	ENSP00000442242.1:p.Pro1300Thr
ENST00000544972.1:c.674C>A
NM_002160.3:c.4987C>A	NP_002151.2:p.Pro1663Thr
XM_005251972.2:c.4714C>A	XP_005252029.1:p.Pro1572Thr
XM_005251973.2:c.4034-4207C>A	XP_005252030.1:n.4034-4207C>A
XM_005251974.2:c.3349C>A	XP_005252031.1:p.Pro1117Thr
XM_005251975.2:c.3215-4207C>A	XP_005252032.1:n.3215-4207C>A
XM_006717096.2:c.5263C>A	XP_006717159.1:p.Pro1755Thr
XM_006717097.2:c.4714C>A	XP_006717160.1:p.Pro1572Thr
XM_006717098.2:c.4441C>A	XP_006717161.1:p.Pro1481Thr
XM_006717100.2:c.4307-4207C>A	XP_006717163.1:n.4307-4207C>A
XM_006717101.2:c.3488-4207C>A	XP_006717164.1:n.3488-4207C>A
XM_011518622.1:c.4990C>A	XP_011516924.1:p.Pro1664Thr
XM_011518623.1:c.4990C>A	XP_011516925.1:p.Pro1664Thr
XM_011518624.1:c.4444C>A	XP_011516926.1:p.Pro1482Thr
XM_011518625.1:c.4580-4207C>A	XP_011516927.1:n.4580-4207C>A
XM_011518626.1:c.4171C>A	XP_011516928.1:p.Pro1391Thr
XM_011518627.1:c.3898C>A	XP_011516929.1:p.Pro1300Thr
XM_011518628.1:c.3761-4207C>A	XP_011516930.1:n.3761-4207C>A
XM_011518629.1:c.3622C>A	XP_011516931.1:p.Pro1208Thr
XM_005251972.4:c.4714C>A	XP_005252029.1:p.Pro1572Thr
XM_005251973.4:c.4034-4207C>A	XP_005252030.1:n.4034-4207C>A
XM_005251974.4:c.3349C>A	XP_005252031.1:p.Pro1117Thr
XM_005251975.4:c.3215-4207C>A	XP_005252032.1:n.3215-4207C>A
XM_006717096.4:c.5263C>A	XP_006717159.1:p.Pro1755Thr
XM_006717097.4:c.4714C>A	XP_006717160.1:p.Pro1572Thr
XM_006717098.4:c.4441C>A	XP_006717161.1:p.Pro1481Thr
XM_006717101.4:c.3488-4207C>A	XP_006717164.1:n.3488-4207C>A
XM_011518625.3:c.4580-4207C>A	XP_011516927.1:n.4580-4207C>A
XM_011518626.3:c.4171C>A	XP_011516928.1:p.Pro1391Thr
XM_011518628.3:c.3761-4207C>A	XP_011516930.1:n.3761-4207C>A
XM_011518629.3:c.3622C>A	XP_011516931.1:p.Pro1208Thr
XM_017014678.2:c.5536C>A	XP_016870167.1:p.Pro1846Thr
XM_017014679.2:c.5263C>A	XP_016870168.1:p.Pro1755Thr
XM_017014680.2:c.5260C>A	XP_016870169.1:p.Pro1754Thr
XM_017014681.2:c.4444C>A	XP_016870170.1:p.Pro1482Thr
XM_024447530.1:c.5536C>A	XP_024303298.1:p.Pro1846Thr
NM_002160.4:c.4987C>A MANE Select	NP_002151.2:p.Pro1663Thr