Canonical Allele Identifier: CA198682277

Gene: TNC

Linked Data

• ClinVar Variation Id: 1267735
• ClinVar RCV Id: RCV001678288
• dbSNP Id: rs3215885
• gnomAD v2: 9-117797359-A-AT
• gnomAD v3: 9-115035080-A-AT
• gnomAD v4: 9-115035080-A-AT
• MyVariant Identifiers: chr9:g.117797360_117797361insT (hg19) ; chr9:g.117797359_117797360insT (hg19) ; chr9:g.115035081_115035082insT (hg38) ; chr9:g.115035080_115035081insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035090dup , CM000671.2:g.115035090dup	GRCh38
NC_000009.11:g.117797369dup , CM000671.1:g.117797369dup	GRCh37
NC_000009.10:g.116837190dup	NCBI36
NG_029637.1:g.88177dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537320.6:c.3876+123dup	ENSP00000443478.1:n.3876+123dup
ENST00000542877.6:c.4698+123dup	ENSP00000442242.1:n.4698+123dup
ENST00000705190.1:c.2730+123dup	ENSP00000516083.1:n.2730+123dup
ENST00000705191.1:c.1386+123dup	ENSP00000516084.1:n.1386+123dup
ENST00000705192.1:c.4745+123dup
ENST00000350763.9:c.5787+123dup MANE Select	ENSP00000265131.4:n.5787+123dup
ENST00000341037.8:c.5241+123dup	ENSP00000339553.4:n.5241+123dup
ENST00000350763.8:c.5787+123dup	ENSP00000265131.4:n.5787+123dup
ENST00000423613.6:c.4968+123dup	ENSP00000411406.2:n.4968+123dup
ENST00000460345.1:n.369+123dup
ENST00000535648.5:c.4698+123dup	ENSP00000438152.2:n.4698+123dup
ENST00000537320.5:c.3876+123dup	ENSP00000443478.1:n.3876+123dup
ENST00000542877.5:c.4698+123dup	ENSP00000442242.1:n.4698+123dup
ENST00000544972.1:c.1474+123dup
NM_002160.3:c.5787+123dup	NP_002151.2:n.5787+123dup
XM_005251972.2:c.5514+123dup	XP_005252029.1:n.5514+123dup
XM_005251973.2:c.4695+123dup	XP_005252030.1:n.4695+123dup
XM_005251974.2:c.4149+123dup	XP_005252031.1:n.4149+123dup
XM_005251975.2:c.3876+123dup	XP_005252032.1:n.3876+123dup
XM_006717096.2:c.6063+123dup	XP_006717159.1:n.6063+123dup
XM_006717097.2:c.5514+123dup	XP_006717160.1:n.5514+123dup
XM_006717098.2:c.5241+123dup	XP_006717161.1:n.5241+123dup
XM_006717100.2:c.4968+123dup	XP_006717163.1:n.4968+123dup
XM_006717101.2:c.4149+123dup	XP_006717164.1:n.4149+123dup
XM_011518622.1:c.5790+123dup	XP_011516924.1:n.5790+123dup
XM_011518623.1:c.5790+123dup	XP_011516925.1:n.5790+123dup
XM_011518624.1:c.5244+123dup	XP_011516926.1:n.5244+123dup
XM_011518625.1:c.5241+123dup	XP_011516927.1:n.5241+123dup
XM_011518626.1:c.4971+123dup	XP_011516928.1:n.4971+123dup
XM_011518627.1:c.4698+123dup	XP_011516929.1:n.4698+123dup
XM_011518628.1:c.4422+123dup	XP_011516930.1:n.4422+123dup
XM_011518629.1:c.4422+123dup	XP_011516931.1:n.4422+123dup
XM_005251972.4:c.5514+123dup	XP_005252029.1:n.5514+123dup
XM_005251973.4:c.4695+123dup	XP_005252030.1:n.4695+123dup
XM_005251974.4:c.4149+123dup	XP_005252031.1:n.4149+123dup
XM_005251975.4:c.3876+123dup	XP_005252032.1:n.3876+123dup
XM_006717096.4:c.6063+123dup	XP_006717159.1:n.6063+123dup
XM_006717097.4:c.5514+123dup	XP_006717160.1:n.5514+123dup
XM_006717098.4:c.5241+123dup	XP_006717161.1:n.5241+123dup
XM_006717101.4:c.4149+123dup	XP_006717164.1:n.4149+123dup
XM_011518625.3:c.5241+123dup	XP_011516927.1:n.5241+123dup
XM_011518626.3:c.4971+123dup	XP_011516928.1:n.4971+123dup
XM_011518628.3:c.4422+123dup	XP_011516930.1:n.4422+123dup
XM_011518629.3:c.4422+123dup	XP_011516931.1:n.4422+123dup
XM_017014678.2:c.6336+123dup	XP_016870167.1:n.6336+123dup
XM_017014679.2:c.6063+123dup	XP_016870168.1:n.6063+123dup
XM_017014680.2:c.6060+123dup	XP_016870169.1:n.6060+123dup
XM_017014681.2:c.5244+123dup	XP_016870170.1:n.5244+123dup
XM_024447530.1:c.6336+123dup	XP_024303298.1:n.6336+123dup
NM_002160.4:c.5787+123dup MANE Select	NP_002151.2:n.5787+123dup