Canonical Allele Identifier: CA374630866

Gene: TNC

Linked Data

• gnomAD v4: 9-115046505-A-G
• MyVariant Identifiers: chr9:g.117808784A>G (hg19) ; chr9:g.115046505A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115046505A>G , CM000671.2:g.115046505A>G	GRCh38
NC_000009.11:g.117808784A>G , CM000671.1:g.117808784A>G	GRCh37
NC_000009.10:g.116848605A>G	NCBI36
NG_029637.1:g.76753T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476680.2:c.318-4164T>C
ENST00000537320.6:c.3215-4164T>C	ENSP00000443478.1:n.3215-4164T>C
ENST00000542877.6:c.3941T>C	ENSP00000442242.1:p.Ile1314Thr
ENST00000705190.1:c.1973T>C	ENSP00000516083.1:p.Ile658Thr
ENST00000705191.1:c.629T>C	ENSP00000516084.1:p.Ile210Thr
ENST00000705192.1:c.3988T>C
ENST00000350763.9:c.5030T>C MANE Select	ENSP00000265131.4:p.Ile1677Thr
ENST00000341037.8:c.4484T>C	ENSP00000339553.4:p.Ile1495Thr
ENST00000350763.8:c.5030T>C	ENSP00000265131.4:p.Ile1677Thr
ENST00000423613.6:c.4307-4164T>C	ENSP00000411406.2:n.4307-4164T>C
ENST00000473855.1:n.348T>C
ENST00000476680.1:n.253-4164T>C
ENST00000498724.5:n.40-4164T>C
ENST00000535648.5:c.3941T>C	ENSP00000438152.2:p.Ile1314Thr
ENST00000537320.5:c.3215-4164T>C	ENSP00000443478.1:n.3215-4164T>C
ENST00000542877.5:c.3941T>C	ENSP00000442242.1:p.Ile1314Thr
ENST00000544972.1:c.717T>C
NM_002160.3:c.5030T>C	NP_002151.2:p.Ile1677Thr
XM_005251972.2:c.4757T>C	XP_005252029.1:p.Ile1586Thr
XM_005251973.2:c.4034-4164T>C	XP_005252030.1:n.4034-4164T>C
XM_005251974.2:c.3392T>C	XP_005252031.1:p.Ile1131Thr
XM_005251975.2:c.3215-4164T>C	XP_005252032.1:n.3215-4164T>C
XM_006717096.2:c.5306T>C	XP_006717159.1:p.Ile1769Thr
XM_006717097.2:c.4757T>C	XP_006717160.1:p.Ile1586Thr
XM_006717098.2:c.4484T>C	XP_006717161.1:p.Ile1495Thr
XM_006717100.2:c.4307-4164T>C	XP_006717163.1:n.4307-4164T>C
XM_006717101.2:c.3488-4164T>C	XP_006717164.1:n.3488-4164T>C
XM_011518622.1:c.5033T>C	XP_011516924.1:p.Ile1678Thr
XM_011518623.1:c.5033T>C	XP_011516925.1:p.Ile1678Thr
XM_011518624.1:c.4487T>C	XP_011516926.1:p.Ile1496Thr
XM_011518625.1:c.4580-4164T>C	XP_011516927.1:n.4580-4164T>C
XM_011518626.1:c.4214T>C	XP_011516928.1:p.Ile1405Thr
XM_011518627.1:c.3941T>C	XP_011516929.1:p.Ile1314Thr
XM_011518628.1:c.3761-4164T>C	XP_011516930.1:n.3761-4164T>C
XM_011518629.1:c.3665T>C	XP_011516931.1:p.Ile1222Thr
XM_005251972.4:c.4757T>C	XP_005252029.1:p.Ile1586Thr
XM_005251973.4:c.4034-4164T>C	XP_005252030.1:n.4034-4164T>C
XM_005251974.4:c.3392T>C	XP_005252031.1:p.Ile1131Thr
XM_005251975.4:c.3215-4164T>C	XP_005252032.1:n.3215-4164T>C
XM_006717096.4:c.5306T>C	XP_006717159.1:p.Ile1769Thr
XM_006717097.4:c.4757T>C	XP_006717160.1:p.Ile1586Thr
XM_006717098.4:c.4484T>C	XP_006717161.1:p.Ile1495Thr
XM_006717101.4:c.3488-4164T>C	XP_006717164.1:n.3488-4164T>C
XM_011518625.3:c.4580-4164T>C	XP_011516927.1:n.4580-4164T>C
XM_011518626.3:c.4214T>C	XP_011516928.1:p.Ile1405Thr
XM_011518628.3:c.3761-4164T>C	XP_011516930.1:n.3761-4164T>C
XM_011518629.3:c.3665T>C	XP_011516931.1:p.Ile1222Thr
XM_017014678.2:c.5579T>C	XP_016870167.1:p.Ile1860Thr
XM_017014679.2:c.5306T>C	XP_016870168.1:p.Ile1769Thr
XM_017014680.2:c.5303T>C	XP_016870169.1:p.Ile1768Thr
XM_017014681.2:c.4487T>C	XP_016870170.1:p.Ile1496Thr
XM_024447530.1:c.5579T>C	XP_024303298.1:p.Ile1860Thr
NM_002160.4:c.5030T>C MANE Select	NP_002151.2:p.Ile1677Thr