Canonical Allele Identifier: CA2691395549

Gene: TNC

Linked Data

• gnomAD v4: 9-115035080-A-AATTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115035080_115035081insATTTTTT , CM000671.2:g.115035080_115035081insATTTTTT	GRCh38
NC_000009.11:g.117797359_117797360insATTTTTT , CM000671.1:g.117797359_117797360insATTTTTT	GRCh37
NC_000009.10:g.116837180_116837181insATTTTTT	NCBI36
NG_029637.1:g.88177_88178insAAAAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537320.6:c.3876+123_3876+124insAAAAAAT	ENSP00000443478.1:n.3876+123_3876+124insAAAAAAT
ENST00000542877.6:c.4698+123_4698+124insAAAAAAT	ENSP00000442242.1:n.4698+123_4698+124insAAAAAAT
ENST00000705190.1:c.2730+123_2730+124insAAAAAAT	ENSP00000516083.1:n.2730+123_2730+124insAAAAAAT
ENST00000705191.1:c.1386+123_1386+124insAAAAAAT	ENSP00000516084.1:n.1386+123_1386+124insAAAAAAT
ENST00000705192.1:c.4745+123_4745+124insAAAAAAT
ENST00000350763.9:c.5787+123_5787+124insAAAAAAT MANE Select	ENSP00000265131.4:n.5787+123_5787+124insAAAAAAT
ENST00000341037.8:c.5241+123_5241+124insAAAAAAT	ENSP00000339553.4:n.5241+123_5241+124insAAAAAAT
ENST00000350763.8:c.5787+123_5787+124insAAAAAAT	ENSP00000265131.4:n.5787+123_5787+124insAAAAAAT
ENST00000423613.6:c.4968+123_4968+124insAAAAAAT	ENSP00000411406.2:n.4968+123_4968+124insAAAAAAT
ENST00000460345.1:n.369+123_369+124insAAAAAAT
ENST00000535648.5:c.4698+123_4698+124insAAAAAAT	ENSP00000438152.2:n.4698+123_4698+124insAAAAAAT
ENST00000537320.5:c.3876+123_3876+124insAAAAAAT	ENSP00000443478.1:n.3876+123_3876+124insAAAAAAT
ENST00000542877.5:c.4698+123_4698+124insAAAAAAT	ENSP00000442242.1:n.4698+123_4698+124insAAAAAAT
ENST00000544972.1:c.1474+123_1474+124insAAAAAAT
NM_002160.3:c.5787+123_5787+124insAAAAAAT	NP_002151.2:n.5787+123_5787+124insAAAAAAT
XM_005251972.2:c.5514+123_5514+124insAAAAAAT	XP_005252029.1:n.5514+123_5514+124insAAAAAAT
XM_005251973.2:c.4695+123_4695+124insAAAAAAT	XP_005252030.1:n.4695+123_4695+124insAAAAAAT
XM_005251974.2:c.4149+123_4149+124insAAAAAAT	XP_005252031.1:n.4149+123_4149+124insAAAAAAT
XM_005251975.2:c.3876+123_3876+124insAAAAAAT	XP_005252032.1:n.3876+123_3876+124insAAAAAAT
XM_006717096.2:c.6063+123_6063+124insAAAAAAT	XP_006717159.1:n.6063+123_6063+124insAAAAAAT
XM_006717097.2:c.5514+123_5514+124insAAAAAAT	XP_006717160.1:n.5514+123_5514+124insAAAAAAT
XM_006717098.2:c.5241+123_5241+124insAAAAAAT	XP_006717161.1:n.5241+123_5241+124insAAAAAAT
XM_006717100.2:c.4968+123_4968+124insAAAAAAT	XP_006717163.1:n.4968+123_4968+124insAAAAAAT
XM_006717101.2:c.4149+123_4149+124insAAAAAAT	XP_006717164.1:n.4149+123_4149+124insAAAAAAT
XM_011518622.1:c.5790+123_5790+124insAAAAAAT	XP_011516924.1:n.5790+123_5790+124insAAAAAAT
XM_011518623.1:c.5790+123_5790+124insAAAAAAT	XP_011516925.1:n.5790+123_5790+124insAAAAAAT
XM_011518624.1:c.5244+123_5244+124insAAAAAAT	XP_011516926.1:n.5244+123_5244+124insAAAAAAT
XM_011518625.1:c.5241+123_5241+124insAAAAAAT	XP_011516927.1:n.5241+123_5241+124insAAAAAAT
XM_011518626.1:c.4971+123_4971+124insAAAAAAT	XP_011516928.1:n.4971+123_4971+124insAAAAAAT
XM_011518627.1:c.4698+123_4698+124insAAAAAAT	XP_011516929.1:n.4698+123_4698+124insAAAAAAT
XM_011518628.1:c.4422+123_4422+124insAAAAAAT	XP_011516930.1:n.4422+123_4422+124insAAAAAAT
XM_011518629.1:c.4422+123_4422+124insAAAAAAT	XP_011516931.1:n.4422+123_4422+124insAAAAAAT
XM_005251972.4:c.5514+123_5514+124insAAAAAAT	XP_005252029.1:n.5514+123_5514+124insAAAAAAT
XM_005251973.4:c.4695+123_4695+124insAAAAAAT	XP_005252030.1:n.4695+123_4695+124insAAAAAAT
XM_005251974.4:c.4149+123_4149+124insAAAAAAT	XP_005252031.1:n.4149+123_4149+124insAAAAAAT
XM_005251975.4:c.3876+123_3876+124insAAAAAAT	XP_005252032.1:n.3876+123_3876+124insAAAAAAT
XM_006717096.4:c.6063+123_6063+124insAAAAAAT	XP_006717159.1:n.6063+123_6063+124insAAAAAAT
XM_006717097.4:c.5514+123_5514+124insAAAAAAT	XP_006717160.1:n.5514+123_5514+124insAAAAAAT
XM_006717098.4:c.5241+123_5241+124insAAAAAAT	XP_006717161.1:n.5241+123_5241+124insAAAAAAT
XM_006717101.4:c.4149+123_4149+124insAAAAAAT	XP_006717164.1:n.4149+123_4149+124insAAAAAAT
XM_011518625.3:c.5241+123_5241+124insAAAAAAT	XP_011516927.1:n.5241+123_5241+124insAAAAAAT
XM_011518626.3:c.4971+123_4971+124insAAAAAAT	XP_011516928.1:n.4971+123_4971+124insAAAAAAT
XM_011518628.3:c.4422+123_4422+124insAAAAAAT	XP_011516930.1:n.4422+123_4422+124insAAAAAAT
XM_011518629.3:c.4422+123_4422+124insAAAAAAT	XP_011516931.1:n.4422+123_4422+124insAAAAAAT
XM_017014678.2:c.6336+123_6336+124insAAAAAAT	XP_016870167.1:n.6336+123_6336+124insAAAAAAT
XM_017014679.2:c.6063+123_6063+124insAAAAAAT	XP_016870168.1:n.6063+123_6063+124insAAAAAAT
XM_017014680.2:c.6060+123_6060+124insAAAAAAT	XP_016870169.1:n.6060+123_6060+124insAAAAAAT
XM_017014681.2:c.5244+123_5244+124insAAAAAAT	XP_016870170.1:n.5244+123_5244+124insAAAAAAT
XM_024447530.1:c.6336+123_6336+124insAAAAAAT	XP_024303298.1:n.6336+123_6336+124insAAAAAAT
NM_002160.4:c.5787+123_5787+124insAAAAAAT MANE Select	NP_002151.2:n.5787+123_5787+124insAAAAAAT