Canonical Allele Identifier: CA374626585

Gene: TNC

Linked Data

• MyVariant Identifiers: chr9:g.117797583G>C (hg19) ; chr9:g.115035304G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035304G>C , CM000671.2:g.115035304G>C	GRCh38
NC_000009.11:g.117797583G>C , CM000671.1:g.117797583G>C	GRCh37
NC_000009.10:g.116837404G>C	NCBI36
NG_029637.1:g.87954C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537320.6:c.3776C>G	ENSP00000443478.1:p.Thr1259Ser
ENST00000542877.6:c.4598C>G	ENSP00000442242.1:p.Thr1533Ser
ENST00000705190.1:c.2630C>G	ENSP00000516083.1:p.Thr877Ser
ENST00000705191.1:c.1286C>G	ENSP00000516084.1:p.Thr429Ser
ENST00000705192.1:c.4645C>G
ENST00000350763.9:c.5687C>G MANE Select	ENSP00000265131.4:p.Thr1896Ser
ENST00000341037.8:c.5141C>G	ENSP00000339553.4:p.Thr1714Ser
ENST00000350763.8:c.5687C>G	ENSP00000265131.4:p.Thr1896Ser
ENST00000423613.6:c.4868C>G	ENSP00000411406.2:p.Thr1623Ser
ENST00000460345.1:n.269C>G
ENST00000535648.5:c.4598C>G	ENSP00000438152.2:p.Thr1533Ser
ENST00000537320.5:c.3776C>G	ENSP00000443478.1:p.Thr1259Ser
ENST00000542877.5:c.4598C>G	ENSP00000442242.1:p.Thr1533Ser
ENST00000544972.1:c.1374C>G
NM_002160.3:c.5687C>G	NP_002151.2:p.Thr1896Ser
XM_005251972.2:c.5414C>G	XP_005252029.1:p.Thr1805Ser
XM_005251973.2:c.4595C>G	XP_005252030.1:p.Thr1532Ser
XM_005251974.2:c.4049C>G	XP_005252031.1:p.Thr1350Ser
XM_005251975.2:c.3776C>G	XP_005252032.1:p.Thr1259Ser
XM_006717096.2:c.5963C>G	XP_006717159.1:p.Thr1988Ser
XM_006717097.2:c.5414C>G	XP_006717160.1:p.Thr1805Ser
XM_006717098.2:c.5141C>G	XP_006717161.1:p.Thr1714Ser
XM_006717100.2:c.4868C>G	XP_006717163.1:p.Thr1623Ser
XM_006717101.2:c.4049C>G	XP_006717164.1:p.Thr1350Ser
XM_011518622.1:c.5690C>G	XP_011516924.1:p.Thr1897Ser
XM_011518623.1:c.5690C>G	XP_011516925.1:p.Thr1897Ser
XM_011518624.1:c.5144C>G	XP_011516926.1:p.Thr1715Ser
XM_011518625.1:c.5141C>G	XP_011516927.1:p.Thr1714Ser
XM_011518626.1:c.4871C>G	XP_011516928.1:p.Thr1624Ser
XM_011518627.1:c.4598C>G	XP_011516929.1:p.Thr1533Ser
XM_011518628.1:c.4322C>G	XP_011516930.1:p.Thr1441Ser
XM_011518629.1:c.4322C>G	XP_011516931.1:p.Thr1441Ser
XM_005251972.4:c.5414C>G	XP_005252029.1:p.Thr1805Ser
XM_005251973.4:c.4595C>G	XP_005252030.1:p.Thr1532Ser
XM_005251974.4:c.4049C>G	XP_005252031.1:p.Thr1350Ser
XM_005251975.4:c.3776C>G	XP_005252032.1:p.Thr1259Ser
XM_006717096.4:c.5963C>G	XP_006717159.1:p.Thr1988Ser
XM_006717097.4:c.5414C>G	XP_006717160.1:p.Thr1805Ser
XM_006717098.4:c.5141C>G	XP_006717161.1:p.Thr1714Ser
XM_006717101.4:c.4049C>G	XP_006717164.1:p.Thr1350Ser
XM_011518625.3:c.5141C>G	XP_011516927.1:p.Thr1714Ser
XM_011518626.3:c.4871C>G	XP_011516928.1:p.Thr1624Ser
XM_011518628.3:c.4322C>G	XP_011516930.1:p.Thr1441Ser
XM_011518629.3:c.4322C>G	XP_011516931.1:p.Thr1441Ser
XM_017014678.2:c.6236C>G	XP_016870167.1:p.Thr2079Ser
XM_017014679.2:c.5963C>G	XP_016870168.1:p.Thr1988Ser
XM_017014680.2:c.5960C>G	XP_016870169.1:p.Thr1987Ser
XM_017014681.2:c.5144C>G	XP_016870170.1:p.Thr1715Ser
XM_024447530.1:c.6236C>G	XP_024303298.1:p.Thr2079Ser
NM_002160.4:c.5687C>G MANE Select	NP_002151.2:p.Thr1896Ser