Canonical Allele Identifier: CA2610226516

Gene: LGI1

Linked Data

• gnomAD v4: 10-93793060-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793060_93793061insAA , CM000672.2:g.93793060_93793061insAA	GRCh38
NC_000010.10:g.95552817_95552818insAA , CM000672.1:g.95552817_95552818insAA	GRCh37
NC_000010.9:g.95542807_95542808insAA	NCBI36
NG_011832.1:g.40252_40253insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.674-126_674-125insAA MANE Select	ENSP00000360472.4:n.674-126_674-125insAA
ENST00000485458.3:n.4650-126_4650-125insAA
ENST00000635953.1:c.674-126_674-125insAA	ENSP00000490058.1:n.674-126_674-125insAA
ENST00000636155.1:c.674-126_674-125insAA	ENSP00000490355.1:n.674-126_674-125insAA
ENST00000636232.1:c.*460-126_*460-125insAA	ENSP00000490325.1:n.*460-126_*460-125insAA
ENST00000636754.1:c.*516-126_*516-125insAA	ENSP00000489781.1:n.*516-126_*516-125insAA
ENST00000636946.1:c.*843-126_*843-125insAA	ENSP00000490654.1:n.*843-126_*843-125insAA
ENST00000637037.1:c.*264-126_*264-125insAA	ENSP00000490860.1:n.*264-126_*264-125insAA
ENST00000637347.1:n.535-126_535-125insAA
ENST00000637611.1:c.*230-126_*230-125insAA	ENSP00000489682.1:n.*230-126_*230-125insAA
ENST00000637689.1:c.-698-126_-698-125insAA	ENSP00000490496.1:n.-698-126_-698-125insAA
ENST00000637925.1:c.*269-126_*269-125insAA	ENSP00000489763.1:n.*269-126_*269-125insAA
ENST00000638049.1:c.*432-126_*432-125insAA	ENSP00000490597.1:n.*432-126_*432-125insAA
ENST00000676175.1:n.2413-126_2413-125insAA
ENST00000371413.4:c.674-126_674-125insAA	ENSP00000360467.3:n.674-126_674-125insAA
ENST00000371418.8:c.674-126_674-125insAA	ENSP00000360472.4:n.674-126_674-125insAA
ENST00000626307.1:n.4589-126_4589-125insAA
ENST00000626946.1:n.218_219insAA
ENST00000627420.2:c.*383-126_*383-125insAA	ENSP00000487116.1:n.*383-126_*383-125insAA
ENST00000629035.2:c.602-126_602-125insAA	ENSP00000486908.1:n.602-126_602-125insAA
ENST00000630047.2:c.530-126_530-125insAA	ENSP00000485917.1:n.530-126_530-125insAA
ENST00000630412.1:n.462-126_462-125insAA
ENST00000630487.2:c.*464-126_*464-125insAA	ENSP00000486859.1:n.*464-126_*464-125insAA
NM_001308275.1:c.674-126_674-125insAA	NP_001295204.1:n.674-126_674-125insAA
NM_001308276.1:c.530-126_530-125insAA	NP_001295205.1:n.530-126_530-125insAA
NM_005097.2:c.674-126_674-125insAA	NP_005088.1:n.674-126_674-125insAA
NM_005097.3:c.674-126_674-125insAA	NP_005088.1:n.674-126_674-125insAA
NR_131777.1:n.938-126_938-125insAA
XM_017016911.2:c.674-126_674-125insAA	XP_016872400.1:n.674-126_674-125insAA
XM_017016912.2:c.530-126_530-125insAA	XP_016872401.1:n.530-126_530-125insAA
NM_005097.4:c.674-126_674-125insAA MANE Select	NP_005088.1:n.674-126_674-125insAA
NM_001308275.2:c.674-126_674-125insAA	NP_001295204.1:n.674-126_674-125insAA
NM_001308276.2:c.530-126_530-125insAA	NP_001295205.1:n.530-126_530-125insAA
NR_131777.2:n.811-126_811-125insAA