Canonical Allele Identifier: CA198707303

Gene: TNC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.115062673_115062674del , CM000671.2:g.115062673_115062674del	GRCh38
NC_000009.11:g.117824952_117824953del , CM000671.1:g.117824952_117824953del	GRCh37
NC_000009.10:g.116864773_116864774del	NCBI36
NG_029637.1:g.60594_60595del

Transcript Alleles

HGVS	Amino-acid Change
NM_002160.4:c.4033+253_4033+254del MANE Select	NP_002151.2:n.4033+253_4033+254del
ENST00000350763.9:c.4033+253_4033+254del MANE Select	ENSP00000265131.4:n.4033+253_4033+254del
NM_002160.3:c.4033+253_4033+254del	NP_002151.2:n.4033+253_4033+254del
ENST00000341037.8:c.3760+1132_3760+1133del	ENSP00000339553.4:n.3760+1132_3760+1133del
ENST00000350763.8:c.4033+253_4033+254del	ENSP00000265131.4:n.4033+253_4033+254del
ENST00000423613.6:c.4033+253_4033+254del	ENSP00000411406.2:n.4033+253_4033+254del
ENST00000473855.1:n.170+10939_170+10940del
ENST00000476680.1:n.252+253_252+254del
ENST00000476680.2:c.317+253_317+254del
ENST00000498724.5:n.39+10939_39+10940del
ENST00000535648.5:c.3215-5239_3215-5238del	ENSP00000438152.2:n.3215-5239_3215-5238del
ENST00000537320.5:c.3214+10939_3214+10940del	ENSP00000443478.1:n.3214+10939_3214+10940del
ENST00000537320.6:c.3214+10939_3214+10940del	ENSP00000443478.1:n.3214+10939_3214+10940del
ENST00000542877.5:c.3215-5239_3215-5238del	ENSP00000442242.1:n.3215-5239_3215-5238del
ENST00000542877.6:c.3215-5239_3215-5238del	ENSP00000442242.1:n.3215-5239_3215-5238del
ENST00000544972.1:c.266+1983_266+1984del
ENST00000705190.1:c.703+253_703+254del	ENSP00000516083.1:n.703+253_703+254del
ENST00000705191.1:c.178+10939_178+10940del	ENSP00000516084.1:n.178+10939_178+10940del
ENST00000705192.1:c.3264+253_3264+254del
XM_005251972.2:c.4033+253_4033+254del	XP_005252029.1:n.4033+253_4033+254del
XM_005251972.4:c.4033+253_4033+254del	XP_005252029.1:n.4033+253_4033+254del
XM_005251973.2:c.4033+253_4033+254del	XP_005252030.1:n.4033+253_4033+254del
XM_005251973.4:c.4033+253_4033+254del	XP_005252030.1:n.4033+253_4033+254del
XM_005251974.2:c.3214+10939_3214+10940del	XP_005252031.1:n.3214+10939_3214+10940del
XM_005251974.4:c.3214+10939_3214+10940del	XP_005252031.1:n.3214+10939_3214+10940del
XM_005251975.2:c.3214+10939_3214+10940del	XP_005252032.1:n.3214+10939_3214+10940del
XM_005251975.4:c.3214+10939_3214+10940del	XP_005252032.1:n.3214+10939_3214+10940del
XM_006717096.2:c.4033+253_4033+254del	XP_006717159.1:n.4033+253_4033+254del
XM_006717096.4:c.4033+253_4033+254del	XP_006717159.1:n.4033+253_4033+254del
XM_006717097.2:c.3760+1132_3760+1133del	XP_006717160.1:n.3760+1132_3760+1133del
XM_006717097.4:c.3760+1132_3760+1133del	XP_006717160.1:n.3760+1132_3760+1133del
XM_006717098.2:c.3760+1132_3760+1133del	XP_006717161.1:n.3760+1132_3760+1133del
XM_006717098.4:c.3760+1132_3760+1133del	XP_006717161.1:n.3760+1132_3760+1133del
XM_006717100.2:c.4033+253_4033+254del	XP_006717163.1:n.4033+253_4033+254del
XM_006717101.2:c.3487+1983_3487+1984del	XP_006717164.1:n.3487+1983_3487+1984del
XM_006717101.4:c.3487+1983_3487+1984del	XP_006717164.1:n.3487+1983_3487+1984del
XM_011518622.1:c.4033+253_4033+254del	XP_011516924.1:n.4033+253_4033+254del
XM_011518623.1:c.3760+1132_3760+1133del	XP_011516925.1:n.3760+1132_3760+1133del
XM_011518624.1:c.3252+2218_3252+2219del	XP_011516926.1:n.3252+2218_3252+2219del
XM_011518625.1:c.4033+253_4033+254del	XP_011516927.1:n.4033+253_4033+254del
XM_011518625.3:c.4033+253_4033+254del	XP_011516927.1:n.4033+253_4033+254del
XM_011518626.1:c.3215-5239_3215-5238del	XP_011516928.1:n.3215-5239_3215-5238del
XM_011518626.3:c.3215-5239_3215-5238del	XP_011516928.1:n.3215-5239_3215-5238del
XM_011518627.1:c.3215-5239_3215-5238del	XP_011516929.1:n.3215-5239_3215-5238del
XM_011518628.1:c.3760+1132_3760+1133del	XP_011516930.1:n.3760+1132_3760+1133del
XM_011518628.3:c.3760+1132_3760+1133del	XP_011516930.1:n.3760+1132_3760+1133del
XM_011518629.1:c.3215-5239_3215-5238del	XP_011516931.1:n.3215-5239_3215-5238del
XM_011518629.3:c.3215-5239_3215-5238del	XP_011516931.1:n.3215-5239_3215-5238del
XM_011518630.1:c.4033+253_4033+254del	XP_011516932.1:n.4033+253_4033+254del
XM_017014678.2:c.4033+253_4033+254del	XP_016870167.1:n.4033+253_4033+254del
XM_017014679.2:c.3760+1132_3760+1133del	XP_016870168.1:n.3760+1132_3760+1133del
XM_017014680.2:c.4033+253_4033+254del	XP_016870169.1:n.4033+253_4033+254del
XM_017014681.2:c.3215-5239_3215-5238del	XP_016870170.1:n.3215-5239_3215-5238del
XM_024447530.1:c.4033+253_4033+254del	XP_024303298.1:n.4033+253_4033+254del