Canonical Allele Identifier: CA198685597
Community Standard Title: NM_002160.4(TNC):c.5249-225del
Gene: TNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.115041309del , CM000671.2:g.115041309del GRCh38
NC_000009.11:g.117803588del , CM000671.1:g.117803588del GRCh37
NC_000009.10:g.116843409del NCBI36
NG_029637.1:g.81949del

Transcript Alleles

HGVS Amino-acid Change
NM_002160.4:c.5249-225del MANE Select NP_002151.2:n.5249-225del
ENST00000350763.9:c.5249-225del MANE Select ENSP00000265131.4:n.5249-225del
NM_002160.3:c.5249-225del NP_002151.2:n.5249-225del
ENST00000341037.8:c.4703-225del ENSP00000339553.4:n.4703-225del
ENST00000350763.8:c.5249-225del ENSP00000265131.4:n.5249-225del
ENST00000423613.6:c.4430-225del ENSP00000411406.2:n.4430-225del
ENST00000476680.1:n.376-225del
ENST00000476680.2:c.441-225del
ENST00000498724.5:n.163-225del
ENST00000535648.5:c.4160-225del ENSP00000438152.2:n.4160-225del
ENST00000537320.5:c.3338-225del ENSP00000443478.1:n.3338-225del
ENST00000537320.6:c.3338-225del ENSP00000443478.1:n.3338-225del
ENST00000542877.5:c.4160-225del ENSP00000442242.1:n.4160-225del
ENST00000542877.6:c.4160-225del ENSP00000442242.1:n.4160-225del
ENST00000544972.1:c.936-225del
ENST00000705190.1:c.2192-225del ENSP00000516083.1:n.2192-225del
ENST00000705191.1:c.848-225del ENSP00000516084.1:n.848-225del
ENST00000705192.1:c.4207-225del
XM_005251972.2:c.4976-225del XP_005252029.1:n.4976-225del
XM_005251972.4:c.4976-225del XP_005252029.1:n.4976-225del
XM_005251973.2:c.4157-225del XP_005252030.1:n.4157-225del
XM_005251973.4:c.4157-225del XP_005252030.1:n.4157-225del
XM_005251974.2:c.3611-225del XP_005252031.1:n.3611-225del
XM_005251974.4:c.3611-225del XP_005252031.1:n.3611-225del
XM_005251975.2:c.3338-225del XP_005252032.1:n.3338-225del
XM_005251975.4:c.3338-225del XP_005252032.1:n.3338-225del
XM_006717096.2:c.5525-225del XP_006717159.1:n.5525-225del
XM_006717096.4:c.5525-225del XP_006717159.1:n.5525-225del
XM_006717097.2:c.4976-225del XP_006717160.1:n.4976-225del
XM_006717097.4:c.4976-225del XP_006717160.1:n.4976-225del
XM_006717098.2:c.4703-225del XP_006717161.1:n.4703-225del
XM_006717098.4:c.4703-225del XP_006717161.1:n.4703-225del
XM_006717100.2:c.4430-225del XP_006717163.1:n.4430-225del
XM_006717101.2:c.3611-225del XP_006717164.1:n.3611-225del
XM_006717101.4:c.3611-225del XP_006717164.1:n.3611-225del
XM_011518622.1:c.5252-225del XP_011516924.1:n.5252-225del
XM_011518623.1:c.5252-225del XP_011516925.1:n.5252-225del
XM_011518624.1:c.4706-225del XP_011516926.1:n.4706-225del
XM_011518625.1:c.4703-225del XP_011516927.1:n.4703-225del
XM_011518625.3:c.4703-225del XP_011516927.1:n.4703-225del
XM_011518626.1:c.4433-225del XP_011516928.1:n.4433-225del
XM_011518626.3:c.4433-225del XP_011516928.1:n.4433-225del
XM_011518627.1:c.4160-225del XP_011516929.1:n.4160-225del
XM_011518628.1:c.3884-225del XP_011516930.1:n.3884-225del
XM_011518628.3:c.3884-225del XP_011516930.1:n.3884-225del
XM_011518629.1:c.3884-225del XP_011516931.1:n.3884-225del
XM_011518629.3:c.3884-225del XP_011516931.1:n.3884-225del
XM_017014678.2:c.5798-225del XP_016870167.1:n.5798-225del
XM_017014679.2:c.5525-225del XP_016870168.1:n.5525-225del
XM_017014680.2:c.5522-225del XP_016870169.1:n.5522-225del
XM_017014681.2:c.4706-225del XP_016870170.1:n.4706-225del
XM_024447530.1:c.5798-225del XP_024303298.1:n.5798-225del