Canonical Allele Identifier: CA377626740

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556850C>T (hg19) ; chr10:g.93797093C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797093C>T , CM000672.2:g.93797093C>T	GRCh38
NC_000010.10:g.95556850C>T , CM000672.1:g.95556850C>T	GRCh37
NC_000010.9:g.95546840C>T	NCBI36
NG_011832.1:g.44285C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.964C>T MANE Select	ENSP00000360472.4:p.Gln322Ter
ENST00000485458.3:n.4940C>T
ENST00000635804.1:n.398C>T
ENST00000635953.1:c.*386C>T	ENSP00000490058.1:n.*386C>T
ENST00000636155.1:c.838+3743C>T	ENSP00000490355.1:n.838+3743C>T
ENST00000636232.1:c.*750C>T	ENSP00000490325.1:n.*750C>T
ENST00000636754.1:c.*806C>T	ENSP00000489781.1:n.*806C>T
ENST00000636946.1:c.*1008-656C>T	ENSP00000490654.1:n.*1008-656C>T
ENST00000637037.1:c.*554C>T	ENSP00000490860.1:n.*554C>T
ENST00000637347.1:n.825C>T
ENST00000637611.1:c.*520C>T	ENSP00000489682.1:n.*520C>T
ENST00000637689.1:c.-408C>T	ENSP00000490496.1:n.-408C>T
ENST00000637925.1:c.*559C>T	ENSP00000489763.1:n.*559C>T
ENST00000638049.1:c.*722C>T	ENSP00000490597.1:n.*722C>T
ENST00000676175.1:n.2703C>T
ENST00000371413.4:c.839-656C>T	ENSP00000360467.3:n.839-656C>T
ENST00000371418.8:c.964C>T	ENSP00000360472.4:p.Gln322Ter
ENST00000626307.1:n.4879C>T
ENST00000627420.2:c.*673C>T	ENSP00000487116.1:n.*673C>T
ENST00000629035.2:c.892C>T	ENSP00000486908.1:p.Gln298Ter
ENST00000630047.2:c.820C>T	ENSP00000485917.1:p.Gln274Ter
NM_001308275.1:c.839-656C>T	NP_001295204.1:n.839-656C>T
NM_001308276.1:c.820C>T	NP_001295205.1:p.Gln274Ter
NM_005097.2:c.964C>T	NP_005088.1:p.Gln322Ter
NM_005097.3:c.964C>T	NP_005088.1:p.Gln322Ter
NR_131777.1:n.1228C>T
XM_017016912.2:c.695-656C>T	XP_016872401.1:n.695-656C>T
NM_005097.4:c.964C>T MANE Select	NP_005088.1:p.Gln322Ter
NM_001308275.2:c.839-656C>T	NP_001295204.1:n.839-656C>T
NM_001308276.2:c.820C>T	NP_001295205.1:p.Gln274Ter
NR_131777.2:n.1101C>T