Canonical Allele Identifier: CA2679972365

Gene: FIG4

Linked Data

• gnomAD v4: 6-109792544-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109792544A>G , CM000668.2:g.109792544A>G	GRCh38
NC_000006.11:g.110113747A>G , CM000668.1:g.110113747A>G	GRCh37
NC_000006.10:g.110220440A>G	NCBI36
NG_007977.1:g.106324A>G , LRG_241:g.106324A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230124.8:c.2377-38A>G MANE Select	ENSP00000230124.4:n.2377-38A>G
ENST00000415980.2:c.883-38A>G	ENSP00000405660.2:n.883-38A>G
ENST00000419951.2:n.725-38A>G
ENST00000674532.1:n.5573-38A>G
ENST00000674557.1:c.*1670-38A>G	ENSP00000501608.1:n.*1670-38A>G
ENST00000674569.1:c.*1496-38A>G	ENSP00000502769.1:n.*1496-38A>G
ENST00000674571.1:c.*1496-38A>G	ENSP00000501633.1:n.*1496-38A>G
ENST00000674575.1:c.*1496-38A>G	ENSP00000502276.1:n.*1496-38A>G
ENST00000674641.1:c.2032-38A>G	ENSP00000501609.1:n.2032-38A>G
ENST00000674644.1:c.1447-38A>G	ENSP00000502201.1:n.1447-38A>G
ENST00000674649.1:c.*2070-38A>G	ENSP00000501669.1:n.*2070-38A>G
ENST00000674657.1:c.*1809-38A>G	ENSP00000502314.1:n.*1809-38A>G
ENST00000674744.1:c.2371-38A>G	ENSP00000501661.1:n.2371-38A>G
ENST00000674778.1:c.*1595-38A>G	ENSP00000502742.1:n.*1595-38A>G
ENST00000674783.1:c.*1292-38A>G	ENSP00000502755.1:n.*1292-38A>G
ENST00000674884.1:c.2395-38A>G	ENSP00000502668.1:n.2395-38A>G
ENST00000674930.1:c.*1502-38A>G	ENSP00000502657.1:n.*1502-38A>G
ENST00000674933.1:c.2146-38A>G	ENSP00000502376.1:n.2146-38A>G
ENST00000674956.1:c.*1591-38A>G	ENSP00000501904.1:n.*1591-38A>G
ENST00000675004.1:c.*2329-38A>G	ENSP00000501868.1:n.*2329-38A>G
ENST00000675009.1:c.*1761-38A>G	ENSP00000502098.1:n.*1761-38A>G
ENST00000675096.1:c.2170-38A>G	ENSP00000502116.1:n.2170-38A>G
ENST00000675122.1:c.*484-38A>G	ENSP00000501810.1:n.*484-38A>G
ENST00000675153.1:c.*1094-38A>G	ENSP00000501682.1:n.*1094-38A>G
ENST00000675254.1:n.3798A>G
ENST00000675272.1:n.6675-38A>G
ENST00000675284.1:c.2377-38A>G	ENSP00000502758.1:n.2377-38A>G
ENST00000675301.1:n.1034-38A>G
ENST00000675311.1:c.*1579-38A>G	ENSP00000501961.1:n.*1579-38A>G
ENST00000675426.1:c.*1445-38A>G	ENSP00000501819.1:n.*1445-38A>G
ENST00000675523.1:c.2146-38A>G	ENSP00000502384.1:n.2146-38A>G
ENST00000675552.1:c.*4640-38A>G	ENSP00000502197.1:n.*4640-38A>G
ENST00000675726.1:c.2377-38A>G	ENSP00000502452.1:n.2377-38A>G
ENST00000675772.1:c.2377-38A>G	ENSP00000501678.1:n.2377-38A>G
ENST00000675831.1:c.1984-38A>G	ENSP00000502382.1:n.1984-38A>G
ENST00000675849.1:n.1999-38A>G
ENST00000675879.1:c.1222-38A>G
ENST00000675887.1:c.*1980-38A>G	ENSP00000502123.1:n.*1980-38A>G
ENST00000675954.1:n.3710-38A>G
ENST00000675991.1:c.*4166A>G	ENSP00000502162.1:n.*4166A>G
ENST00000675994.1:c.*1516-38A>G	ENSP00000502419.1:n.*1516-38A>G
ENST00000676021.1:c.*955-38A>G	ENSP00000502746.1:n.*955-38A>G
ENST00000676037.1:c.*304-38A>G	ENSP00000502181.1:n.*304-38A>G
ENST00000676136.1:n.5024-38A>G
ENST00000676246.1:n.267-38A>G
ENST00000676442.1:c.2248-38A>G	ENSP00000502595.1:n.2248-38A>G
ENST00000230124.7:c.2377-38A>G	ENSP00000230124.3:n.2377-38A>G
NM_014845.5:c.2377-38A>G , LRG_241t1:c.2377-38A>G	NP_055660.1:n.2377-38A>G
XM_011536281.1:c.2314-38A>G	XP_011534583.1:n.2314-38A>G
XM_011536281.3:c.2314-38A>G	XP_011534583.1:n.2314-38A>G
XM_017011592.1:c.1828-38A>G	XP_016867081.1:n.1828-38A>G
XM_017011593.2:c.1447-38A>G	XP_016867082.1:n.1447-38A>G
NM_014845.6:c.2377-38A>G MANE Select	NP_055660.1:n.2377-38A>G