Canonical Allele Identifier: CA2610227022

Gene: LGI1

Linked Data

• gnomAD v4: 10-93793457-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793460_93793461del , CM000672.2:g.93793460_93793461del	GRCh38
NC_000010.10:g.95553217_95553218del , CM000672.1:g.95553217_95553218del	GRCh37
NC_000010.9:g.95543207_95543208del	NCBI36
NG_011832.1:g.40652_40653del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.838+110_838+111del MANE Select	ENSP00000360472.4:n.838+110_838+111del
ENST00000485458.3:n.4814+110_4814+111del
ENST00000635953.1:c.838+110_838+111del	ENSP00000490058.1:n.838+110_838+111del
ENST00000636155.1:c.838+110_838+111del	ENSP00000490355.1:n.838+110_838+111del
ENST00000636232.1:c.*624+110_*624+111del	ENSP00000490325.1:n.*624+110_*624+111del
ENST00000636754.1:c.*680+110_*680+111del	ENSP00000489781.1:n.*680+110_*680+111del
ENST00000636946.1:c.*1007+110_*1007+111del	ENSP00000490654.1:n.*1007+110_*1007+111del
ENST00000637037.1:c.*428+110_*428+111del	ENSP00000490860.1:n.*428+110_*428+111del
ENST00000637347.1:n.699+110_699+111del
ENST00000637611.1:c.*394+110_*394+111del	ENSP00000489682.1:n.*394+110_*394+111del
ENST00000637689.1:c.-534+110_-534+111del	ENSP00000490496.1:n.-534+110_-534+111del
ENST00000637925.1:c.*433+110_*433+111del	ENSP00000489763.1:n.*433+110_*433+111del
ENST00000638049.1:c.*596+110_*596+111del	ENSP00000490597.1:n.*596+110_*596+111del
ENST00000676175.1:n.2577+110_2577+111del
ENST00000371413.4:c.838+110_838+111del	ENSP00000360467.3:n.838+110_838+111del
ENST00000371418.8:c.838+110_838+111del	ENSP00000360472.4:n.838+110_838+111del
ENST00000626307.1:n.4753+110_4753+111del
ENST00000626946.1:n.508+110_508+111del
ENST00000627420.2:c.*547+110_*547+111del	ENSP00000487116.1:n.*547+110_*547+111del
ENST00000629035.2:c.766+110_766+111del	ENSP00000486908.1:n.766+110_766+111del
ENST00000630047.2:c.694+110_694+111del	ENSP00000485917.1:n.694+110_694+111del
NM_001308275.1:c.838+110_838+111del	NP_001295204.1:n.838+110_838+111del
NM_001308276.1:c.694+110_694+111del	NP_001295205.1:n.694+110_694+111del
NM_005097.2:c.838+110_838+111del	NP_005088.1:n.838+110_838+111del
NM_005097.3:c.838+110_838+111del	NP_005088.1:n.838+110_838+111del
NR_131777.1:n.1102+110_1102+111del
XM_017016911.2:c.838+110_838+111del	XP_016872400.1:n.838+110_838+111del
XM_017016912.2:c.694+110_694+111del	XP_016872401.1:n.694+110_694+111del
NM_005097.4:c.838+110_838+111del MANE Select	NP_005088.1:n.838+110_838+111del
NM_001308275.2:c.838+110_838+111del	NP_001295204.1:n.838+110_838+111del
NM_001308276.2:c.694+110_694+111del	NP_001295205.1:n.694+110_694+111del
NR_131777.2:n.975+110_975+111del