Canonical Allele Identifier: CA365228450

Gene: FIG4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109766728G>T , CM000668.2:g.109766728G>T	GRCh38
NC_000006.11:g.110087931G>T , CM000668.1:g.110087931G>T	GRCh37
NC_000006.10:g.110194624G>T	NCBI36
NG_007977.1:g.80508G>T , LRG_241:g.80508G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014845.6:c.1584-1G>T MANE Select	NP_055660.1:n.1584-1G>T
ENST00000230124.8:c.1584-1G>T MANE Select	ENSP00000230124.4:n.1584-1G>T
NM_014845.5:c.1584-1G>T , LRG_241t1:c.1584-1G>T	NP_055660.1:n.1584-1G>T
ENST00000230124.7:c.1584-1G>T	ENSP00000230124.3:n.1584-1G>T
ENST00000415980.2:c.90-1G>T	ENSP00000405660.2:n.90-1G>T
ENST00000674532.1:n.4780-1G>T
ENST00000674557.1:c.*1016-1G>T	ENSP00000501608.1:n.*1016-1G>T
ENST00000674569.1:c.*703-1G>T	ENSP00000502769.1:n.*703-1G>T
ENST00000674571.1:c.*703-1G>T	ENSP00000501633.1:n.*703-1G>T
ENST00000674575.1:c.*703-1G>T	ENSP00000502276.1:n.*703-1G>T
ENST00000674641.1:c.1239-1G>T	ENSP00000501609.1:n.1239-1G>T
ENST00000674644.1:c.654-1G>T	ENSP00000502201.1:n.654-1G>T
ENST00000674649.1:c.*1277-1G>T	ENSP00000501669.1:n.*1277-1G>T
ENST00000674657.1:c.*1016-1G>T	ENSP00000502314.1:n.*1016-1G>T
ENST00000674744.1:c.1578-1G>T	ENSP00000501661.1:n.1578-1G>T
ENST00000674778.1:c.*703-1G>T	ENSP00000502742.1:n.*703-1G>T
ENST00000674783.1:c.*499-1G>T	ENSP00000502755.1:n.*499-1G>T
ENST00000674884.1:c.1602-1G>T	ENSP00000502668.1:n.1602-1G>T
ENST00000674930.1:c.*709-1G>T	ENSP00000502657.1:n.*709-1G>T
ENST00000674933.1:c.1353-1G>T	ENSP00000502376.1:n.1353-1G>T
ENST00000674956.1:c.*798-1G>T	ENSP00000501904.1:n.*798-1G>T
ENST00000675004.1:c.*1536-1G>T	ENSP00000501868.1:n.*1536-1G>T
ENST00000675009.1:c.*968-1G>T	ENSP00000502098.1:n.*968-1G>T
ENST00000675096.1:c.1584-1G>T	ENSP00000502116.1:n.1584-1G>T
ENST00000675122.1:c.1584-1G>T	ENSP00000501810.1:n.1584-1G>T
ENST00000675153.1:c.*301-1G>T	ENSP00000501682.1:n.*301-1G>T
ENST00000675272.1:n.5882-1G>T
ENST00000675284.1:c.1584-1G>T	ENSP00000502758.1:n.1584-1G>T
ENST00000675301.1:n.241-1G>T
ENST00000675311.1:c.*786-1G>T	ENSP00000501961.1:n.*786-1G>T
ENST00000675426.1:c.*652-1G>T	ENSP00000501819.1:n.*652-1G>T
ENST00000675523.1:c.1353-1G>T	ENSP00000502384.1:n.1353-1G>T
ENST00000675552.1:c.*703-1G>T	ENSP00000502197.1:n.*703-1G>T
ENST00000675681.1:c.1584-1G>T	ENSP00000502705.1:n.1584-1G>T
ENST00000675714.1:c.1584-1G>T	ENSP00000502561.1:n.1584-1G>T
ENST00000675726.1:c.1584-1G>T	ENSP00000502452.1:n.1584-1G>T
ENST00000675772.1:c.1584-1G>T	ENSP00000501678.1:n.1584-1G>T
ENST00000675831.1:c.1191-1G>T	ENSP00000502382.1:n.1191-1G>T
ENST00000675847.1:n.1708-1G>T
ENST00000675849.1:n.1206-1G>T
ENST00000675879.1:c.313-1G>T
ENST00000675887.1:c.*1187-1G>T	ENSP00000502123.1:n.*1187-1G>T
ENST00000675973.1:c.1455-1G>T	ENSP00000502407.1:n.1455-1G>T
ENST00000675991.1:c.*703-1G>T	ENSP00000502162.1:n.*703-1G>T
ENST00000675994.1:c.*703-1G>T	ENSP00000502419.1:n.*703-1G>T
ENST00000676021.1:c.*301-1G>T	ENSP00000502746.1:n.*301-1G>T
ENST00000676037.1:c.1584-1G>T	ENSP00000502181.1:n.1584-1G>T
ENST00000676136.1:n.1724-1G>T
ENST00000676442.1:c.1455-1G>T	ENSP00000502595.1:n.1455-1G>T
XM_011536281.1:c.1521-1G>T	XP_011534583.1:n.1521-1G>T
XM_011536281.3:c.1521-1G>T	XP_011534583.1:n.1521-1G>T
XM_017011591.2:c.1584-1G>T	XP_016867080.1:n.1584-1G>T
XM_017011592.1:c.1035-1G>T	XP_016867081.1:n.1035-1G>T
XM_017011593.2:c.654-1G>T	XP_016867082.1:n.654-1G>T