Canonical Allele Identifier: CA670100736

Gene: LGI1

Linked Data

• dbSNP Id: rs1241565642
• MyVariant Identifiers: chr10:g.95553139_95553140del (hg19) ; chr10:g.93793382_93793383del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793382_93793383del , CM000672.2:g.93793382_93793383del	GRCh38
NC_000010.10:g.95553139_95553140del , CM000672.1:g.95553139_95553140del	GRCh37
NC_000010.9:g.95543129_95543130del	NCBI36
NG_011832.1:g.40574_40575del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.838+32_838+33del MANE Select	ENSP00000360472.4:n.838+32_838+33del
ENST00000485458.3:n.4814+32_4814+33del
ENST00000635953.1:c.838+32_838+33del	ENSP00000490058.1:n.838+32_838+33del
ENST00000636155.1:c.838+32_838+33del	ENSP00000490355.1:n.838+32_838+33del
ENST00000636232.1:c.*624+32_*624+33del	ENSP00000490325.1:n.*624+32_*624+33del
ENST00000636754.1:c.*680+32_*680+33del	ENSP00000489781.1:n.*680+32_*680+33del
ENST00000636946.1:c.*1007+32_*1007+33del	ENSP00000490654.1:n.*1007+32_*1007+33del
ENST00000637037.1:c.*428+32_*428+33del	ENSP00000490860.1:n.*428+32_*428+33del
ENST00000637347.1:n.699+32_699+33del
ENST00000637611.1:c.*394+32_*394+33del	ENSP00000489682.1:n.*394+32_*394+33del
ENST00000637689.1:c.-534+32_-534+33del	ENSP00000490496.1:n.-534+32_-534+33del
ENST00000637925.1:c.*433+32_*433+33del	ENSP00000489763.1:n.*433+32_*433+33del
ENST00000638049.1:c.*596+32_*596+33del	ENSP00000490597.1:n.*596+32_*596+33del
ENST00000676175.1:n.2577+32_2577+33del
ENST00000371413.4:c.838+32_838+33del	ENSP00000360467.3:n.838+32_838+33del
ENST00000371418.8:c.838+32_838+33del	ENSP00000360472.4:n.838+32_838+33del
ENST00000626307.1:n.4753+32_4753+33del
ENST00000626946.1:n.508+32_508+33del
ENST00000627420.2:c.*547+32_*547+33del	ENSP00000487116.1:n.*547+32_*547+33del
ENST00000629035.2:c.766+32_766+33del	ENSP00000486908.1:n.766+32_766+33del
ENST00000630047.2:c.694+32_694+33del	ENSP00000485917.1:n.694+32_694+33del
NM_001308275.1:c.838+32_838+33del	NP_001295204.1:n.838+32_838+33del
NM_001308276.1:c.694+32_694+33del	NP_001295205.1:n.694+32_694+33del
NM_005097.2:c.838+32_838+33del	NP_005088.1:n.838+32_838+33del
NM_005097.3:c.838+32_838+33del	NP_005088.1:n.838+32_838+33del
NR_131777.1:n.1102+32_1102+33del
XM_017016911.2:c.838+32_838+33del	XP_016872400.1:n.838+32_838+33del
XM_017016912.2:c.694+32_694+33del	XP_016872401.1:n.694+32_694+33del
NM_005097.4:c.838+32_838+33del MANE Select	NP_005088.1:n.838+32_838+33del
NM_001308275.2:c.838+32_838+33del	NP_001295204.1:n.838+32_838+33del
NM_001308276.2:c.694+32_694+33del	NP_001295205.1:n.694+32_694+33del
NR_131777.2:n.975+32_975+33del