Canonical Allele Identifier: CA2679972417
Gene: FIG4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109792596del , CM000668.2:g.109792596del GRCh38
NC_000006.11:g.110113799del , CM000668.1:g.110113799del GRCh37
NC_000006.10:g.110220492del NCBI36
NG_007977.1:g.106376del , LRG_241:g.106376del

Transcript Alleles

HGVS Amino-acid Change
ENST00000230124.8:c.2391del MANE Select ENSP00000230124.4:p.Met798Ter
ENST00000415980.2:c.897del ENSP00000405660.2:p.Met300Ter
ENST00000419951.2:n.739del
ENST00000674532.1:n.5587del
ENST00000674557.1:c.*1684del ENSP00000501608.1:n.*1684del
ENST00000674569.1:c.*1510del ENSP00000502769.1:n.*1510del
ENST00000674571.1:c.*1510del ENSP00000501633.1:n.*1510del
ENST00000674575.1:c.*1510del ENSP00000502276.1:n.*1510del
ENST00000674641.1:c.2046del ENSP00000501609.1:p.Met683Ter
ENST00000674644.1:c.1461del ENSP00000502201.1:p.Met488Ter
ENST00000674649.1:c.*2084del ENSP00000501669.1:n.*2084del
ENST00000674657.1:c.*1823del ENSP00000502314.1:n.*1823del
ENST00000674744.1:c.2385del ENSP00000501661.1:p.Met796Ter
ENST00000674778.1:c.*1609del ENSP00000502742.1:n.*1609del
ENST00000674783.1:c.*1306del ENSP00000502755.1:n.*1306del
ENST00000674884.1:c.2409del ENSP00000502668.1:p.Met804Ter
ENST00000674930.1:c.*1516del ENSP00000502657.1:n.*1516del
ENST00000674933.1:c.2160del ENSP00000502376.1:p.Met721Ter
ENST00000674956.1:c.*1605del ENSP00000501904.1:n.*1605del
ENST00000675004.1:c.*2343del ENSP00000501868.1:n.*2343del
ENST00000675009.1:c.*1775del ENSP00000502098.1:n.*1775del
ENST00000675096.1:c.2184del ENSP00000502116.1:p.Met729Ter
ENST00000675122.1:c.*498del ENSP00000501810.1:n.*498del
ENST00000675153.1:c.*1108del ENSP00000501682.1:n.*1108del
ENST00000675254.1:n.3850del
ENST00000675272.1:n.6689del
ENST00000675284.1:c.2391del ENSP00000502758.1:p.Met798Ter
ENST00000675301.1:n.1048del
ENST00000675311.1:c.*1593del ENSP00000501961.1:n.*1593del
ENST00000675426.1:c.*1459del ENSP00000501819.1:n.*1459del
ENST00000675523.1:c.2160del ENSP00000502384.1:p.Met721Ter
ENST00000675552.1:c.*4654del ENSP00000502197.1:n.*4654del
ENST00000675726.1:c.2391del ENSP00000502452.1:p.Met798Ter
ENST00000675772.1:c.2391del ENSP00000501678.1:p.Met798Ter
ENST00000675831.1:c.1998del ENSP00000502382.1:p.Met667Ter
ENST00000675849.1:n.2013del
ENST00000675879.1:c.1236del
ENST00000675887.1:c.*1994del ENSP00000502123.1:n.*1994del
ENST00000675954.1:n.3724del
ENST00000675991.1:c.*4218del ENSP00000502162.1:n.*4218del
ENST00000675994.1:c.*1530del ENSP00000502419.1:n.*1530del
ENST00000676021.1:c.*969del ENSP00000502746.1:n.*969del
ENST00000676037.1:c.*318del ENSP00000502181.1:n.*318del
ENST00000676136.1:n.5038del
ENST00000676246.1:n.281del
ENST00000676442.1:c.2262del ENSP00000502595.1:p.Met755Ter
ENST00000230124.7:c.2391del ENSP00000230124.3:p.Met798Ter
NM_014845.5:c.2391del , LRG_241t1:c.2391del NP_055660.1:p.Met798Ter
XM_011536281.1:c.2328del XP_011534583.1:p.Met777Ter
XM_011536281.3:c.2328del XP_011534583.1:p.Met777Ter
XM_017011592.1:c.1842del XP_016867081.1:p.Met615Ter
XM_017011593.2:c.1461del XP_016867082.1:p.Met488Ter
NM_014845.6:c.2391del MANE Select NP_055660.1:p.Met798Ter