Canonical Allele Identifier: CA374626512

Gene: TNC

Linked Data

• gnomAD v4: 9-115035266-G-T
• MyVariant Identifiers: chr9:g.117797545G>T (hg19) ; chr9:g.115035266G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035266G>T , CM000671.2:g.115035266G>T	GRCh38
NC_000009.11:g.117797545G>T , CM000671.1:g.117797545G>T	GRCh37
NC_000009.10:g.116837366G>T	NCBI36
NG_029637.1:g.87992C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537320.6:c.3814C>A	ENSP00000443478.1:p.Pro1272Thr
ENST00000542877.6:c.4636C>A	ENSP00000442242.1:p.Pro1546Thr
ENST00000705190.1:c.2668C>A	ENSP00000516083.1:p.Pro890Thr
ENST00000705191.1:c.1324C>A	ENSP00000516084.1:p.Pro442Thr
ENST00000705192.1:c.4683C>A
ENST00000350763.9:c.5725C>A MANE Select	ENSP00000265131.4:p.Pro1909Thr
ENST00000341037.8:c.5179C>A	ENSP00000339553.4:p.Pro1727Thr
ENST00000350763.8:c.5725C>A	ENSP00000265131.4:p.Pro1909Thr
ENST00000423613.6:c.4906C>A	ENSP00000411406.2:p.Pro1636Thr
ENST00000460345.1:n.307C>A
ENST00000535648.5:c.4636C>A	ENSP00000438152.2:p.Pro1546Thr
ENST00000537320.5:c.3814C>A	ENSP00000443478.1:p.Pro1272Thr
ENST00000542877.5:c.4636C>A	ENSP00000442242.1:p.Pro1546Thr
ENST00000544972.1:c.1412C>A
NM_002160.3:c.5725C>A	NP_002151.2:p.Pro1909Thr
XM_005251972.2:c.5452C>A	XP_005252029.1:p.Pro1818Thr
XM_005251973.2:c.4633C>A	XP_005252030.1:p.Pro1545Thr
XM_005251974.2:c.4087C>A	XP_005252031.1:p.Pro1363Thr
XM_005251975.2:c.3814C>A	XP_005252032.1:p.Pro1272Thr
XM_006717096.2:c.6001C>A	XP_006717159.1:p.Pro2001Thr
XM_006717097.2:c.5452C>A	XP_006717160.1:p.Pro1818Thr
XM_006717098.2:c.5179C>A	XP_006717161.1:p.Pro1727Thr
XM_006717100.2:c.4906C>A	XP_006717163.1:p.Pro1636Thr
XM_006717101.2:c.4087C>A	XP_006717164.1:p.Pro1363Thr
XM_011518622.1:c.5728C>A	XP_011516924.1:p.Pro1910Thr
XM_011518623.1:c.5728C>A	XP_011516925.1:p.Pro1910Thr
XM_011518624.1:c.5182C>A	XP_011516926.1:p.Pro1728Thr
XM_011518625.1:c.5179C>A	XP_011516927.1:p.Pro1727Thr
XM_011518626.1:c.4909C>A	XP_011516928.1:p.Pro1637Thr
XM_011518627.1:c.4636C>A	XP_011516929.1:p.Pro1546Thr
XM_011518628.1:c.4360C>A	XP_011516930.1:p.Pro1454Thr
XM_011518629.1:c.4360C>A	XP_011516931.1:p.Pro1454Thr
XM_005251972.4:c.5452C>A	XP_005252029.1:p.Pro1818Thr
XM_005251973.4:c.4633C>A	XP_005252030.1:p.Pro1545Thr
XM_005251974.4:c.4087C>A	XP_005252031.1:p.Pro1363Thr
XM_005251975.4:c.3814C>A	XP_005252032.1:p.Pro1272Thr
XM_006717096.4:c.6001C>A	XP_006717159.1:p.Pro2001Thr
XM_006717097.4:c.5452C>A	XP_006717160.1:p.Pro1818Thr
XM_006717098.4:c.5179C>A	XP_006717161.1:p.Pro1727Thr
XM_006717101.4:c.4087C>A	XP_006717164.1:p.Pro1363Thr
XM_011518625.3:c.5179C>A	XP_011516927.1:p.Pro1727Thr
XM_011518626.3:c.4909C>A	XP_011516928.1:p.Pro1637Thr
XM_011518628.3:c.4360C>A	XP_011516930.1:p.Pro1454Thr
XM_011518629.3:c.4360C>A	XP_011516931.1:p.Pro1454Thr
XM_017014678.2:c.6274C>A	XP_016870167.1:p.Pro2092Thr
XM_017014679.2:c.6001C>A	XP_016870168.1:p.Pro2001Thr
XM_017014680.2:c.5998C>A	XP_016870169.1:p.Pro2000Thr
XM_017014681.2:c.5182C>A	XP_016870170.1:p.Pro1728Thr
XM_024447530.1:c.6274C>A	XP_024303298.1:p.Pro2092Thr
NM_002160.4:c.5725C>A MANE Select	NP_002151.2:p.Pro1909Thr