Canonical Allele Identifier: CA3956499

Gene: FIG4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109825279C>T , CM000668.2:g.109825279C>T	GRCh38
NC_000006.11:g.110146482C>T , CM000668.1:g.110146482C>T	GRCh37
NC_000006.10:g.110253175C>T	NCBI36
NG_007977.1:g.139059C>T , LRG_241:g.139059C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230124.8:c.*14C>T MANE Select	ENSP00000230124.4:n.*14C>T
ENST00000415980.2:c.*14C>T	ENSP00000405660.2:n.*14C>T
ENST00000674532.1:n.5934C>T
ENST00000674557.1:c.*2031C>T	ENSP00000501608.1:n.*2031C>T
ENST00000674569.1:c.*1857C>T	ENSP00000502769.1:n.*1857C>T
ENST00000674571.1:c.*1882C>T	ENSP00000501633.1:n.*1882C>T
ENST00000674573.1:n.1170C>T
ENST00000674575.1:c.*1857C>T	ENSP00000502276.1:n.*1857C>T
ENST00000674641.1:c.*14C>T	ENSP00000501609.1:n.*14C>T
ENST00000674649.1:c.*2431C>T	ENSP00000501669.1:n.*2431C>T
ENST00000674657.1:c.*2170C>T	ENSP00000502314.1:n.*2170C>T
ENST00000674744.1:c.*14C>T	ENSP00000501661.1:n.*14C>T
ENST00000674778.1:c.*1956C>T	ENSP00000502742.1:n.*1956C>T
ENST00000674783.1:c.*1653C>T	ENSP00000502755.1:n.*1653C>T
ENST00000674884.1:c.*14C>T	ENSP00000502668.1:n.*14C>T
ENST00000674930.1:c.*1776C>T	ENSP00000502657.1:n.*1776C>T
ENST00000674933.1:c.*14C>T	ENSP00000502376.1:n.*14C>T
ENST00000674956.1:c.*1952C>T	ENSP00000501904.1:n.*1952C>T
ENST00000675096.1:c.*14C>T	ENSP00000502116.1:n.*14C>T
ENST00000675122.1:c.*845C>T	ENSP00000501810.1:n.*845C>T
ENST00000675153.1:c.*1455C>T	ENSP00000501682.1:n.*1455C>T
ENST00000675272.1:n.7036C>T
ENST00000675301.1:n.1395C>T
ENST00000675311.1:c.*1940C>T	ENSP00000501961.1:n.*1940C>T
ENST00000675426.1:c.*1806C>T	ENSP00000501819.1:n.*1806C>T
ENST00000675523.1:c.*14C>T	ENSP00000502384.1:n.*14C>T
ENST00000675552.1:c.*5001C>T	ENSP00000502197.1:n.*5001C>T
ENST00000675726.1:c.*14C>T	ENSP00000502452.1:n.*14C>T
ENST00000675772.1:c.2546+28428C>T	ENSP00000501678.1:n.2546+28428C>T
ENST00000675831.1:c.*14C>T	ENSP00000502382.1:n.*14C>T
ENST00000675849.1:n.2360C>T
ENST00000675879.1:c.1583C>T
ENST00000675954.1:n.4071C>T
ENST00000675991.1:c.*4565C>T	ENSP00000502162.1:n.*4565C>T
ENST00000675994.1:c.*1877C>T	ENSP00000502419.1:n.*1877C>T
ENST00000676021.1:c.*1316C>T	ENSP00000502746.1:n.*1316C>T
ENST00000676037.1:c.*665C>T	ENSP00000502181.1:n.*665C>T
ENST00000676136.1:n.5385C>T
ENST00000676442.1:c.*14C>T	ENSP00000502595.1:n.*14C>T
ENST00000230124.7:c.*14C>T	ENSP00000230124.3:n.*14C>T
NM_014845.5:c.*14C>T , LRG_241t1:c.*14C>T	NP_055660.1:n.*14C>T
XM_011536281.1:c.*14C>T	XP_011534583.1:n.*14C>T
XM_011536281.3:c.*14C>T	XP_011534583.1:n.*14C>T
XM_017011592.1:c.*14C>T	XP_016867081.1:n.*14C>T
XM_017011593.2:c.*14C>T	XP_016867082.1:n.*14C>T
NM_014845.6:c.*14C>T MANE Select	NP_055660.1:n.*14C>T