Canonical Allele Identifier: CA12998509

Gene: TNC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115030147G>T , CM000671.2:g.115030147G>T	GRCh38
NC_000009.11:g.117792426G>T , CM000671.1:g.117792426G>T	GRCh37
NC_000009.10:g.116832247G>T	NCBI36
NG_029637.1:g.93111C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002160.4:c.6072+107C>A MANE Select	NP_002151.2:n.6072+107C>A
ENST00000350763.9:c.6072+107C>A MANE Select	ENSP00000265131.4:n.6072+107C>A
NM_002160.3:c.6072+107C>A	NP_002151.2:n.6072+107C>A
ENST00000341037.8:c.5526+107C>A	ENSP00000339553.4:n.5526+107C>A
ENST00000350763.8:c.6072+107C>A	ENSP00000265131.4:n.6072+107C>A
ENST00000423613.6:c.5253+107C>A	ENSP00000411406.2:n.5253+107C>A
ENST00000535648.5:c.4983+107C>A	ENSP00000438152.2:n.4983+107C>A
ENST00000537320.5:c.4161+107C>A	ENSP00000443478.1:n.4161+107C>A
ENST00000537320.6:c.4161+107C>A	ENSP00000443478.1:n.4161+107C>A
ENST00000542877.5:c.4983+107C>A	ENSP00000442242.1:n.4983+107C>A
ENST00000542877.6:c.4983+107C>A	ENSP00000442242.1:n.4983+107C>A
ENST00000544972.1:c.1759+107C>A
ENST00000705190.1:c.3015+107C>A	ENSP00000516083.1:n.3015+107C>A
ENST00000705191.1:c.1671+107C>A	ENSP00000516084.1:n.1671+107C>A
ENST00000705192.1:c.5030+107C>A
XM_005251972.2:c.5799+107C>A	XP_005252029.1:n.5799+107C>A
XM_005251972.4:c.5799+107C>A	XP_005252029.1:n.5799+107C>A
XM_005251973.2:c.4980+107C>A	XP_005252030.1:n.4980+107C>A
XM_005251973.4:c.4980+107C>A	XP_005252030.1:n.4980+107C>A
XM_005251974.2:c.4434+107C>A	XP_005252031.1:n.4434+107C>A
XM_005251974.4:c.4434+107C>A	XP_005252031.1:n.4434+107C>A
XM_005251975.2:c.4161+107C>A	XP_005252032.1:n.4161+107C>A
XM_005251975.4:c.4161+107C>A	XP_005252032.1:n.4161+107C>A
XM_006717096.2:c.6348+107C>A	XP_006717159.1:n.6348+107C>A
XM_006717096.4:c.6348+107C>A	XP_006717159.1:n.6348+107C>A
XM_006717097.2:c.5799+107C>A	XP_006717160.1:n.5799+107C>A
XM_006717097.4:c.5799+107C>A	XP_006717160.1:n.5799+107C>A
XM_006717098.2:c.5526+107C>A	XP_006717161.1:n.5526+107C>A
XM_006717098.4:c.5526+107C>A	XP_006717161.1:n.5526+107C>A
XM_006717100.2:c.5253+107C>A	XP_006717163.1:n.5253+107C>A
XM_006717101.2:c.4434+107C>A	XP_006717164.1:n.4434+107C>A
XM_006717101.4:c.4434+107C>A	XP_006717164.1:n.4434+107C>A
XM_011518622.1:c.6075+107C>A	XP_011516924.1:n.6075+107C>A
XM_011518623.1:c.6075+107C>A	XP_011516925.1:n.6075+107C>A
XM_011518624.1:c.5529+107C>A	XP_011516926.1:n.5529+107C>A
XM_011518625.1:c.5526+107C>A	XP_011516927.1:n.5526+107C>A
XM_011518625.3:c.5526+107C>A	XP_011516927.1:n.5526+107C>A
XM_011518626.1:c.5256+107C>A	XP_011516928.1:n.5256+107C>A
XM_011518626.3:c.5256+107C>A	XP_011516928.1:n.5256+107C>A
XM_011518627.1:c.4983+107C>A	XP_011516929.1:n.4983+107C>A
XM_011518628.1:c.4707+107C>A	XP_011516930.1:n.4707+107C>A
XM_011518628.3:c.4707+107C>A	XP_011516930.1:n.4707+107C>A
XM_011518629.1:c.4707+107C>A	XP_011516931.1:n.4707+107C>A
XM_011518629.3:c.4707+107C>A	XP_011516931.1:n.4707+107C>A
XM_017014678.2:c.6621+107C>A	XP_016870167.1:n.6621+107C>A
XM_017014679.2:c.6348+107C>A	XP_016870168.1:n.6348+107C>A
XM_017014680.2:c.6345+107C>A	XP_016870169.1:n.6345+107C>A
XM_017014681.2:c.5529+107C>A	XP_016870170.1:n.5529+107C>A
XM_024447530.1:c.6621+107C>A	XP_024303298.1:n.6621+107C>A