Canonical Allele Identifier: CA377626673

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556841A>C (hg19) ; chr10:g.93797084A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797084A>C , CM000672.2:g.93797084A>C	GRCh38
NC_000010.10:g.95556841A>C , CM000672.1:g.95556841A>C	GRCh37
NC_000010.9:g.95546831A>C	NCBI36
NG_011832.1:g.44276A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.955A>C MANE Select	ENSP00000360472.4:p.Ile319Leu
ENST00000485458.3:n.4931A>C
ENST00000635804.1:n.389A>C
ENST00000635953.1:c.*377A>C	ENSP00000490058.1:n.*377A>C
ENST00000636155.1:c.838+3734A>C	ENSP00000490355.1:n.838+3734A>C
ENST00000636232.1:c.*741A>C	ENSP00000490325.1:n.*741A>C
ENST00000636754.1:c.*797A>C	ENSP00000489781.1:n.*797A>C
ENST00000636946.1:c.*1008-665A>C	ENSP00000490654.1:n.*1008-665A>C
ENST00000637037.1:c.*545A>C	ENSP00000490860.1:n.*545A>C
ENST00000637347.1:n.816A>C
ENST00000637611.1:c.*511A>C	ENSP00000489682.1:n.*511A>C
ENST00000637689.1:c.-417A>C	ENSP00000490496.1:n.-417A>C
ENST00000637925.1:c.*550A>C	ENSP00000489763.1:n.*550A>C
ENST00000638049.1:c.*713A>C	ENSP00000490597.1:n.*713A>C
ENST00000676175.1:n.2694A>C
ENST00000371413.4:c.839-665A>C	ENSP00000360467.3:n.839-665A>C
ENST00000371418.8:c.955A>C	ENSP00000360472.4:p.Ile319Leu
ENST00000626307.1:n.4870A>C
ENST00000627420.2:c.*664A>C	ENSP00000487116.1:n.*664A>C
ENST00000629035.2:c.883A>C	ENSP00000486908.1:p.Ile295Leu
ENST00000630047.2:c.811A>C	ENSP00000485917.1:p.Ile271Leu
NM_001308275.1:c.839-665A>C	NP_001295204.1:n.839-665A>C
NM_001308276.1:c.811A>C	NP_001295205.1:p.Ile271Leu
NM_005097.2:c.955A>C	NP_005088.1:p.Ile319Leu
NM_005097.3:c.955A>C	NP_005088.1:p.Ile319Leu
NR_131777.1:n.1219A>C
XM_017016912.2:c.695-665A>C	XP_016872401.1:n.695-665A>C
NM_005097.4:c.955A>C MANE Select	NP_005088.1:p.Ile319Leu
NM_001308275.2:c.839-665A>C	NP_001295204.1:n.839-665A>C
NM_001308276.2:c.811A>C	NP_001295205.1:p.Ile271Leu
NR_131777.2:n.1092A>C