Canonical Allele Identifier: CA3955876
Gene: FIG4 HGNC NCBI

Linked Data

dbSNP Id: rs759114524

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109738332del , CM000668.2:g.109738332del GRCh38
NC_000006.11:g.110059535del , CM000668.1:g.110059535del GRCh37
NC_000006.10:g.110166228del NCBI36
NG_007977.1:g.52112del , LRG_241:g.52112del

Transcript Alleles

HGVS Amino-acid Change
ENST00000230124.8:c.654del MANE Select ENSP00000230124.4:p.Phe218LeufsTer9
ENST00000368941.2:c.646+3034del ENSP00000357937.2:n.646+3034del
ENST00000415980.2:c.-223-23759del ENSP00000405660.2:n.-223-23759del
ENST00000454215.6:c.654del ENSP00000412156.2:p.Phe218LeufsTer9
ENST00000674532.1:n.3850del
ENST00000674557.1:c.*86del ENSP00000501608.1:n.*86del
ENST00000674569.1:c.646+3034del ENSP00000502769.1:n.646+3034del
ENST00000674571.1:c.646+3034del ENSP00000501633.1:n.646+3034del
ENST00000674575.1:c.640+3034del ENSP00000502276.1:n.640+3034del
ENST00000674641.1:c.309del ENSP00000501609.1:p.Phe103LeufsTer9
ENST00000674644.1:c.-55+3034del ENSP00000502201.1:n.-55+3034del
ENST00000674649.1:c.*347del ENSP00000501669.1:n.*347del
ENST00000674657.1:c.*86del ENSP00000502314.1:n.*86del
ENST00000674744.1:c.648del ENSP00000501661.1:p.Phe216LeufsTer9
ENST00000674778.1:c.646+3034del ENSP00000502742.1:n.646+3034del
ENST00000674783.1:c.654del ENSP00000502755.1:p.Phe218LeufsTer9
ENST00000674830.1:n.625del
ENST00000674884.1:c.672del ENSP00000502668.1:p.Phe224LeufsTer9
ENST00000674930.1:c.*164+3034del ENSP00000502657.1:n.*164+3034del
ENST00000674933.1:c.423del ENSP00000502376.1:p.Phe141LeufsTer9
ENST00000674956.1:c.646+3034del ENSP00000501904.1:n.646+3034del
ENST00000675002.1:n.742del
ENST00000675004.1:c.*606del ENSP00000501868.1:n.*606del
ENST00000675009.1:c.*172del ENSP00000502098.1:n.*172del
ENST00000675096.1:c.654del ENSP00000502116.1:p.Phe218LeufsTer9
ENST00000675122.1:c.654del ENSP00000501810.1:p.Phe218LeufsTer9
ENST00000675153.1:c.654del ENSP00000501682.1:p.Phe218LeufsTer9
ENST00000675272.1:n.1560del
ENST00000675284.1:c.654del ENSP00000502758.1:p.Phe218LeufsTer9
ENST00000675311.1:c.*78+3034del ENSP00000501961.1:n.*78+3034del
ENST00000675426.1:c.*78+3034del ENSP00000501819.1:n.*78+3034del
ENST00000675523.1:c.423del ENSP00000502384.1:p.Phe141LeufsTer9
ENST00000675552.1:c.646+3034del ENSP00000502197.1:n.646+3034del
ENST00000675681.1:c.654del ENSP00000502705.1:p.Phe218LeufsTer9
ENST00000675714.1:c.654del ENSP00000502561.1:p.Phe218LeufsTer9
ENST00000675726.1:c.654del ENSP00000502452.1:p.Phe218LeufsTer9
ENST00000675772.1:c.654del ENSP00000501678.1:p.Phe218LeufsTer9
ENST00000675831.1:c.646+3034del ENSP00000502382.1:n.646+3034del
ENST00000675844.1:c.423del ENSP00000502353.1:p.Phe141LeufsTer9
ENST00000675847.1:n.778del
ENST00000675887.1:c.*257del ENSP00000502123.1:n.*257del
ENST00000675973.1:c.646+3034del ENSP00000502407.1:n.646+3034del
ENST00000675991.1:c.646+3034del ENSP00000502162.1:n.646+3034del
ENST00000675994.1:c.646+3034del ENSP00000502419.1:n.646+3034del
ENST00000676021.1:c.654del ENSP00000502746.1:p.Phe218LeufsTer9
ENST00000676037.1:c.654del ENSP00000502181.1:p.Phe218LeufsTer9
ENST00000676136.1:n.794del
ENST00000676435.1:c.654del ENSP00000502614.1:p.Phe218LeufsTer9
ENST00000676442.1:c.646+3034del ENSP00000502595.1:n.646+3034del
ENST00000230124.7:c.654del ENSP00000230124.3:p.Phe218LeufsTer9
ENST00000368941.1:c.415+3034del ENSP00000357937.1:n.415+3034del
ENST00000454215.5:c.591del ENSP00000412156.1:p.Phe197LeufsTer9
NM_014845.5:c.654del , LRG_241t1:c.654del NP_055660.1:p.Phe218LeufsTer9
XM_011536281.1:c.591del XP_011534583.1:p.Phe197LeufsTer9
XM_011536281.3:c.591del XP_011534583.1:p.Phe197LeufsTer9
XM_017011591.2:c.654del XP_016867080.1:p.Phe218LeufsTer9
XM_017011592.1:c.105del XP_016867081.1:p.Phe35LeufsTer9
XM_017011593.2:c.-55+3034del XP_016867082.1:n.-55+3034del
NM_014845.6:c.654del MANE Select NP_055660.1:p.Phe218LeufsTer9