Canonical Allele Identifier: CA1874112765

Gene: TNC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115033117_115033118delinsTA , CM000671.2:g.115033117_115033118delinsTA	GRCh38
NC_000009.11:g.117795396_117795397delinsTA , CM000671.1:g.117795396_117795397delinsTA	GRCh37
NC_000009.10:g.116835217_116835218delinsTA	NCBI36
NG_029637.1:g.90140_90141delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537320.6:c.3877-1433_3877-1432delinsTA	ENSP00000443478.1:n.3877-1433_3877-1432delinsTA
ENST00000542877.6:c.4699-1433_4699-1432delinsTA	ENSP00000442242.1:n.4699-1433_4699-1432delinsTA
ENST00000705190.1:c.2731-1433_2731-1432delinsTA	ENSP00000516083.1:n.2731-1433_2731-1432delinsTA
ENST00000705191.1:c.1387-1433_1387-1432delinsTA	ENSP00000516084.1:n.1387-1433_1387-1432delinsTA
ENST00000705192.1:c.4746-1433_4746-1432delinsTA
ENST00000350763.9:c.5788-1433_5788-1432delinsTA MANE Select	ENSP00000265131.4:n.5788-1433_5788-1432delinsTA
ENST00000341037.8:c.5242-1433_5242-1432delinsTA	ENSP00000339553.4:n.5242-1433_5242-1432delinsTA
ENST00000350763.8:c.5788-1433_5788-1432delinsTA	ENSP00000265131.4:n.5788-1433_5788-1432delinsTA
ENST00000423613.6:c.4969-1433_4969-1432delinsTA	ENSP00000411406.2:n.4969-1433_4969-1432delinsTA
ENST00000460345.1:n.370-1433_370-1432delinsTA
ENST00000535648.5:c.4699-1433_4699-1432delinsTA	ENSP00000438152.2:n.4699-1433_4699-1432delinsTA
ENST00000537320.5:c.3877-1433_3877-1432delinsTA	ENSP00000443478.1:n.3877-1433_3877-1432delinsTA
ENST00000542877.5:c.4699-1433_4699-1432delinsTA	ENSP00000442242.1:n.4699-1433_4699-1432delinsTA
ENST00000544972.1:c.1475-1433_1475-1432delinsTA
NM_002160.3:c.5788-1433_5788-1432delinsTA	NP_002151.2:n.5788-1433_5788-1432delinsTA
XM_005251972.2:c.5515-1433_5515-1432delinsTA	XP_005252029.1:n.5515-1433_5515-1432delinsTA
XM_005251973.2:c.4696-1433_4696-1432delinsTA	XP_005252030.1:n.4696-1433_4696-1432delinsTA
XM_005251974.2:c.4150-1433_4150-1432delinsTA	XP_005252031.1:n.4150-1433_4150-1432delinsTA
XM_005251975.2:c.3877-1433_3877-1432delinsTA	XP_005252032.1:n.3877-1433_3877-1432delinsTA
XM_006717096.2:c.6064-1433_6064-1432delinsTA	XP_006717159.1:n.6064-1433_6064-1432delinsTA
XM_006717097.2:c.5515-1433_5515-1432delinsTA	XP_006717160.1:n.5515-1433_5515-1432delinsTA
XM_006717098.2:c.5242-1433_5242-1432delinsTA	XP_006717161.1:n.5242-1433_5242-1432delinsTA
XM_006717100.2:c.4969-1433_4969-1432delinsTA	XP_006717163.1:n.4969-1433_4969-1432delinsTA
XM_006717101.2:c.4150-1433_4150-1432delinsTA	XP_006717164.1:n.4150-1433_4150-1432delinsTA
XM_011518622.1:c.5791-1433_5791-1432delinsTA	XP_011516924.1:n.5791-1433_5791-1432delinsTA
XM_011518623.1:c.5791-1433_5791-1432delinsTA	XP_011516925.1:n.5791-1433_5791-1432delinsTA
XM_011518624.1:c.5245-1433_5245-1432delinsTA	XP_011516926.1:n.5245-1433_5245-1432delinsTA
XM_011518625.1:c.5242-1433_5242-1432delinsTA	XP_011516927.1:n.5242-1433_5242-1432delinsTA
XM_011518626.1:c.4972-1433_4972-1432delinsTA	XP_011516928.1:n.4972-1433_4972-1432delinsTA
XM_011518627.1:c.4699-1433_4699-1432delinsTA	XP_011516929.1:n.4699-1433_4699-1432delinsTA
XM_011518628.1:c.4423-1433_4423-1432delinsTA	XP_011516930.1:n.4423-1433_4423-1432delinsTA
XM_011518629.1:c.4423-1433_4423-1432delinsTA	XP_011516931.1:n.4423-1433_4423-1432delinsTA
XM_005251972.4:c.5515-1433_5515-1432delinsTA	XP_005252029.1:n.5515-1433_5515-1432delinsTA
XM_005251973.4:c.4696-1433_4696-1432delinsTA	XP_005252030.1:n.4696-1433_4696-1432delinsTA
XM_005251974.4:c.4150-1433_4150-1432delinsTA	XP_005252031.1:n.4150-1433_4150-1432delinsTA
XM_005251975.4:c.3877-1433_3877-1432delinsTA	XP_005252032.1:n.3877-1433_3877-1432delinsTA
XM_006717096.4:c.6064-1433_6064-1432delinsTA	XP_006717159.1:n.6064-1433_6064-1432delinsTA
XM_006717097.4:c.5515-1433_5515-1432delinsTA	XP_006717160.1:n.5515-1433_5515-1432delinsTA
XM_006717098.4:c.5242-1433_5242-1432delinsTA	XP_006717161.1:n.5242-1433_5242-1432delinsTA
XM_006717101.4:c.4150-1433_4150-1432delinsTA	XP_006717164.1:n.4150-1433_4150-1432delinsTA
XM_011518625.3:c.5242-1433_5242-1432delinsTA	XP_011516927.1:n.5242-1433_5242-1432delinsTA
XM_011518626.3:c.4972-1433_4972-1432delinsTA	XP_011516928.1:n.4972-1433_4972-1432delinsTA
XM_011518628.3:c.4423-1433_4423-1432delinsTA	XP_011516930.1:n.4423-1433_4423-1432delinsTA
XM_011518629.3:c.4423-1433_4423-1432delinsTA	XP_011516931.1:n.4423-1433_4423-1432delinsTA
XM_017014678.2:c.6337-1433_6337-1432delinsTA	XP_016870167.1:n.6337-1433_6337-1432delinsTA
XM_017014679.2:c.6064-1433_6064-1432delinsTA	XP_016870168.1:n.6064-1433_6064-1432delinsTA
XM_017014680.2:c.6061-1433_6061-1432delinsTA	XP_016870169.1:n.6061-1433_6061-1432delinsTA
XM_017014681.2:c.5245-1433_5245-1432delinsTA	XP_016870170.1:n.5245-1433_5245-1432delinsTA
XM_024447530.1:c.6337-1433_6337-1432delinsTA	XP_024303298.1:n.6337-1433_6337-1432delinsTA
NM_002160.4:c.5788-1433_5788-1432delinsTA MANE Select	NP_002151.2:n.5788-1433_5788-1432delinsTA