Canonical Allele Identifier: CA143925
Gene: FIG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 50996
dbSNP Id: rs397514707

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109735176T>C , CM000668.2:g.109735176T>C GRCh38
NC_000006.11:g.110056379T>C , CM000668.1:g.110056379T>C GRCh37
NC_000006.10:g.110163072T>C NCBI36
NG_007977.1:g.48956T>C , LRG_241:g.48956T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000230124.8:c.524T>C MANE Select ENSP00000230124.4:p.Leu175Pro
ENST00000368941.2:c.524T>C ENSP00000357937.2:p.Leu175Pro
ENST00000415980.2:c.-223-26915T>C ENSP00000405660.2:n.-223-26915T>C
ENST00000454215.6:c.524T>C ENSP00000412156.2:p.Leu175Pro
ENST00000674532.1:n.694T>C
ENST00000674557.1:c.367T>C ENSP00000501608.1:p.Phe123Leu
ENST00000674569.1:c.524T>C ENSP00000502769.1:p.Leu175Pro
ENST00000674571.1:c.524T>C ENSP00000501633.1:p.Leu175Pro
ENST00000674575.1:c.518T>C ENSP00000502276.1:p.Leu173Pro
ENST00000674614.1:n.491T>C
ENST00000674641.1:c.179T>C ENSP00000501609.1:p.Leu60Pro
ENST00000674644.1:c.-177T>C ENSP00000502201.1:n.-177T>C
ENST00000674649.1:c.*217T>C ENSP00000501669.1:n.*217T>C
ENST00000674657.1:c.367T>C ENSP00000502314.1:p.Phe123Leu
ENST00000674744.1:c.518T>C ENSP00000501661.1:p.Leu173Pro
ENST00000674778.1:c.524T>C ENSP00000502742.1:p.Leu175Pro
ENST00000674783.1:c.524T>C ENSP00000502755.1:p.Leu175Pro
ENST00000674830.1:n.495T>C
ENST00000674884.1:c.542T>C ENSP00000502668.1:p.Leu181Pro
ENST00000674930.1:c.*42T>C ENSP00000502657.1:n.*42T>C
ENST00000674933.1:c.293T>C ENSP00000502376.1:p.Leu98Pro
ENST00000674956.1:c.524T>C ENSP00000501904.1:p.Leu175Pro
ENST00000675002.1:n.612T>C
ENST00000675004.1:c.*476T>C ENSP00000501868.1:n.*476T>C
ENST00000675009.1:c.*42T>C ENSP00000502098.1:n.*42T>C
ENST00000675096.1:c.524T>C ENSP00000502116.1:p.Leu175Pro
ENST00000675122.1:c.524T>C ENSP00000501810.1:p.Leu175Pro
ENST00000675153.1:c.524T>C ENSP00000501682.1:p.Leu175Pro
ENST00000675284.1:c.524T>C ENSP00000502758.1:p.Leu175Pro
ENST00000675311.1:c.367T>C ENSP00000501961.1:p.Phe123Leu
ENST00000675426.1:c.367T>C ENSP00000501819.1:p.Phe123Leu
ENST00000675523.1:c.293T>C ENSP00000502384.1:p.Leu98Pro
ENST00000675552.1:c.524T>C ENSP00000502197.1:p.Leu175Pro
ENST00000675681.1:c.524T>C ENSP00000502705.1:p.Leu175Pro
ENST00000675714.1:c.524T>C ENSP00000502561.1:p.Leu175Pro
ENST00000675726.1:c.524T>C ENSP00000502452.1:p.Leu175Pro
ENST00000675772.1:c.524T>C ENSP00000501678.1:p.Leu175Pro
ENST00000675831.1:c.524T>C ENSP00000502382.1:p.Leu175Pro
ENST00000675834.1:n.362T>C
ENST00000675844.1:c.293T>C ENSP00000502353.1:p.Leu98Pro
ENST00000675847.1:n.648T>C
ENST00000675887.1:c.*127T>C ENSP00000502123.1:n.*127T>C
ENST00000675973.1:c.524T>C ENSP00000502407.1:p.Leu175Pro
ENST00000675991.1:c.524T>C ENSP00000502162.1:p.Leu175Pro
ENST00000675994.1:c.524T>C ENSP00000502419.1:p.Leu175Pro
ENST00000676021.1:c.524T>C ENSP00000502746.1:p.Leu175Pro
ENST00000676037.1:c.524T>C ENSP00000502181.1:p.Leu175Pro
ENST00000676136.1:n.664T>C
ENST00000676435.1:c.524T>C ENSP00000502614.1:p.Leu175Pro
ENST00000676442.1:c.524T>C ENSP00000502595.1:p.Leu175Pro
ENST00000230124.7:c.524T>C ENSP00000230124.3:p.Leu175Pro
ENST00000368941.1:c.293T>C ENSP00000357937.1:p.Leu98Pro
ENST00000454215.5:c.461T>C ENSP00000412156.1:p.Leu154Pro
NM_014845.5:c.524T>C , LRG_241t1:c.524T>C NP_055660.1:p.Leu175Pro
XM_011536281.1:c.461T>C XP_011534583.1:p.Leu154Pro
XM_011536281.3:c.461T>C XP_011534583.1:p.Leu154Pro
XM_017011591.2:c.524T>C XP_016867080.1:p.Leu175Pro
XM_017011592.1:c.-26T>C XP_016867081.1:n.-26T>C
XM_017011593.2:c.-177T>C XP_016867082.1:n.-177T>C
NM_014845.6:c.524T>C MANE Select NP_055660.1:p.Leu175Pro