Canonical Allele Identifier: CA2610227006

Gene: LGI1

Linked Data

• gnomAD v4: 10-93793444-CATTTGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793448_93793453del , CM000672.2:g.93793448_93793453del	GRCh38
NC_000010.10:g.95553205_95553210del , CM000672.1:g.95553205_95553210del	GRCh37
NC_000010.9:g.95543195_95543200del	NCBI36
NG_011832.1:g.40640_40645del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.838+98_838+103del MANE Select	ENSP00000360472.4:n.838+98_838+103del
ENST00000485458.3:n.4814+98_4814+103del
ENST00000635953.1:c.838+98_838+103del	ENSP00000490058.1:n.838+98_838+103del
ENST00000636155.1:c.838+98_838+103del	ENSP00000490355.1:n.838+98_838+103del
ENST00000636232.1:c.*624+98_*624+103del	ENSP00000490325.1:n.*624+98_*624+103del
ENST00000636754.1:c.*680+98_*680+103del	ENSP00000489781.1:n.*680+98_*680+103del
ENST00000636946.1:c.*1007+98_*1007+103del	ENSP00000490654.1:n.*1007+98_*1007+103del
ENST00000637037.1:c.*428+98_*428+103del	ENSP00000490860.1:n.*428+98_*428+103del
ENST00000637347.1:n.699+98_699+103del
ENST00000637611.1:c.*394+98_*394+103del	ENSP00000489682.1:n.*394+98_*394+103del
ENST00000637689.1:c.-534+98_-534+103del	ENSP00000490496.1:n.-534+98_-534+103del
ENST00000637925.1:c.*433+98_*433+103del	ENSP00000489763.1:n.*433+98_*433+103del
ENST00000638049.1:c.*596+98_*596+103del	ENSP00000490597.1:n.*596+98_*596+103del
ENST00000676175.1:n.2577+98_2577+103del
ENST00000371413.4:c.838+98_838+103del	ENSP00000360467.3:n.838+98_838+103del
ENST00000371418.8:c.838+98_838+103del	ENSP00000360472.4:n.838+98_838+103del
ENST00000626307.1:n.4753+98_4753+103del
ENST00000626946.1:n.508+98_508+103del
ENST00000627420.2:c.*547+98_*547+103del	ENSP00000487116.1:n.*547+98_*547+103del
ENST00000629035.2:c.766+98_766+103del	ENSP00000486908.1:n.766+98_766+103del
ENST00000630047.2:c.694+98_694+103del	ENSP00000485917.1:n.694+98_694+103del
NM_001308275.1:c.838+98_838+103del	NP_001295204.1:n.838+98_838+103del
NM_001308276.1:c.694+98_694+103del	NP_001295205.1:n.694+98_694+103del
NM_005097.2:c.838+98_838+103del	NP_005088.1:n.838+98_838+103del
NM_005097.3:c.838+98_838+103del	NP_005088.1:n.838+98_838+103del
NR_131777.1:n.1102+98_1102+103del
XM_017016911.2:c.838+98_838+103del	XP_016872400.1:n.838+98_838+103del
XM_017016912.2:c.694+98_694+103del	XP_016872401.1:n.694+98_694+103del
NM_005097.4:c.838+98_838+103del MANE Select	NP_005088.1:n.838+98_838+103del
NM_001308275.2:c.838+98_838+103del	NP_001295204.1:n.838+98_838+103del
NM_001308276.2:c.694+98_694+103del	NP_001295205.1:n.694+98_694+103del
NR_131777.2:n.975+98_975+103del