Canonical Allele Identifier: CA374626446

Gene: TNC

Linked Data

• MyVariant Identifiers: chr9:g.117797508T>G (hg19) ; chr9:g.115035229T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035229T>G , CM000671.2:g.115035229T>G	GRCh38
NC_000009.11:g.117797508T>G , CM000671.1:g.117797508T>G	GRCh37
NC_000009.10:g.116837329T>G	NCBI36
NG_029637.1:g.88029A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000537320.6:c.3851A>C	ENSP00000443478.1:p.Tyr1284Ser
ENST00000542877.6:c.4673A>C	ENSP00000442242.1:p.Tyr1558Ser
ENST00000705190.1:c.2705A>C	ENSP00000516083.1:p.Tyr902Ser
ENST00000705191.1:c.1361A>C	ENSP00000516084.1:p.Tyr454Ser
ENST00000705192.1:c.4720A>C
ENST00000350763.9:c.5762A>C MANE Select	ENSP00000265131.4:p.Tyr1921Ser
ENST00000341037.8:c.5216A>C	ENSP00000339553.4:p.Tyr1739Ser
ENST00000350763.8:c.5762A>C	ENSP00000265131.4:p.Tyr1921Ser
ENST00000423613.6:c.4943A>C	ENSP00000411406.2:p.Tyr1648Ser
ENST00000460345.1:n.344A>C
ENST00000535648.5:c.4673A>C	ENSP00000438152.2:p.Tyr1558Ser
ENST00000537320.5:c.3851A>C	ENSP00000443478.1:p.Tyr1284Ser
ENST00000542877.5:c.4673A>C	ENSP00000442242.1:p.Tyr1558Ser
ENST00000544972.1:c.1449A>C
NM_002160.3:c.5762A>C	NP_002151.2:p.Tyr1921Ser
XM_005251972.2:c.5489A>C	XP_005252029.1:p.Tyr1830Ser
XM_005251973.2:c.4670A>C	XP_005252030.1:p.Tyr1557Ser
XM_005251974.2:c.4124A>C	XP_005252031.1:p.Tyr1375Ser
XM_005251975.2:c.3851A>C	XP_005252032.1:p.Tyr1284Ser
XM_006717096.2:c.6038A>C	XP_006717159.1:p.Tyr2013Ser
XM_006717097.2:c.5489A>C	XP_006717160.1:p.Tyr1830Ser
XM_006717098.2:c.5216A>C	XP_006717161.1:p.Tyr1739Ser
XM_006717100.2:c.4943A>C	XP_006717163.1:p.Tyr1648Ser
XM_006717101.2:c.4124A>C	XP_006717164.1:p.Tyr1375Ser
XM_011518622.1:c.5765A>C	XP_011516924.1:p.Tyr1922Ser
XM_011518623.1:c.5765A>C	XP_011516925.1:p.Tyr1922Ser
XM_011518624.1:c.5219A>C	XP_011516926.1:p.Tyr1740Ser
XM_011518625.1:c.5216A>C	XP_011516927.1:p.Tyr1739Ser
XM_011518626.1:c.4946A>C	XP_011516928.1:p.Tyr1649Ser
XM_011518627.1:c.4673A>C	XP_011516929.1:p.Tyr1558Ser
XM_011518628.1:c.4397A>C	XP_011516930.1:p.Tyr1466Ser
XM_011518629.1:c.4397A>C	XP_011516931.1:p.Tyr1466Ser
XM_005251972.4:c.5489A>C	XP_005252029.1:p.Tyr1830Ser
XM_005251973.4:c.4670A>C	XP_005252030.1:p.Tyr1557Ser
XM_005251974.4:c.4124A>C	XP_005252031.1:p.Tyr1375Ser
XM_005251975.4:c.3851A>C	XP_005252032.1:p.Tyr1284Ser
XM_006717096.4:c.6038A>C	XP_006717159.1:p.Tyr2013Ser
XM_006717097.4:c.5489A>C	XP_006717160.1:p.Tyr1830Ser
XM_006717098.4:c.5216A>C	XP_006717161.1:p.Tyr1739Ser
XM_006717101.4:c.4124A>C	XP_006717164.1:p.Tyr1375Ser
XM_011518625.3:c.5216A>C	XP_011516927.1:p.Tyr1739Ser
XM_011518626.3:c.4946A>C	XP_011516928.1:p.Tyr1649Ser
XM_011518628.3:c.4397A>C	XP_011516930.1:p.Tyr1466Ser
XM_011518629.3:c.4397A>C	XP_011516931.1:p.Tyr1466Ser
XM_017014678.2:c.6311A>C	XP_016870167.1:p.Tyr2104Ser
XM_017014679.2:c.6038A>C	XP_016870168.1:p.Tyr2013Ser
XM_017014680.2:c.6035A>C	XP_016870169.1:p.Tyr2012Ser
XM_017014681.2:c.5219A>C	XP_016870170.1:p.Tyr1740Ser
XM_024447530.1:c.6311A>C	XP_024303298.1:p.Tyr2104Ser
NM_002160.4:c.5762A>C MANE Select	NP_002151.2:p.Tyr1921Ser