Canonical Allele Identifier: CA2610226454

Gene: LGI1

Linked Data

• gnomAD v4: 10-93793011-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793011G>C , CM000672.2:g.93793011G>C	GRCh38
NC_000010.10:g.95552768G>C , CM000672.1:g.95552768G>C	GRCh37
NC_000010.9:g.95542758G>C	NCBI36
NG_011832.1:g.40203G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.673+99G>C MANE Select	ENSP00000360472.4:n.673+99G>C
ENST00000485458.3:n.4649+99G>C
ENST00000635953.1:c.673+99G>C	ENSP00000490058.1:n.673+99G>C
ENST00000636155.1:c.673+99G>C	ENSP00000490355.1:n.673+99G>C
ENST00000636232.1:c.*459+99G>C	ENSP00000490325.1:n.*459+99G>C
ENST00000636754.1:c.*515+99G>C	ENSP00000489781.1:n.*515+99G>C
ENST00000636946.1:c.*842+99G>C	ENSP00000490654.1:n.*842+99G>C
ENST00000637037.1:c.*263+99G>C	ENSP00000490860.1:n.*263+99G>C
ENST00000637347.1:n.534+99G>C
ENST00000637611.1:c.*229+99G>C	ENSP00000489682.1:n.*229+99G>C
ENST00000637689.1:c.-699+99G>C	ENSP00000490496.1:n.-699+99G>C
ENST00000637925.1:c.*268+99G>C	ENSP00000489763.1:n.*268+99G>C
ENST00000638049.1:c.*431+99G>C	ENSP00000490597.1:n.*431+99G>C
ENST00000676175.1:n.2412+99G>C
ENST00000371413.4:c.673+99G>C	ENSP00000360467.3:n.673+99G>C
ENST00000371418.8:c.673+99G>C	ENSP00000360472.4:n.673+99G>C
ENST00000626307.1:n.4588+99G>C
ENST00000626946.1:n.169G>C
ENST00000627420.2:c.*382+99G>C	ENSP00000487116.1:n.*382+99G>C
ENST00000629035.2:c.601+99G>C	ENSP00000486908.1:n.601+99G>C
ENST00000630047.2:c.529+99G>C	ENSP00000485917.1:n.529+99G>C
ENST00000630412.1:n.461+99G>C
ENST00000630487.2:c.*463+99G>C	ENSP00000486859.1:n.*463+99G>C
NM_001308275.1:c.673+99G>C	NP_001295204.1:n.673+99G>C
NM_001308276.1:c.529+99G>C	NP_001295205.1:n.529+99G>C
NM_005097.2:c.673+99G>C	NP_005088.1:n.673+99G>C
NM_005097.3:c.673+99G>C	NP_005088.1:n.673+99G>C
NR_131777.1:n.937+99G>C
XM_017016911.2:c.673+99G>C	XP_016872400.1:n.673+99G>C
XM_017016912.2:c.529+99G>C	XP_016872401.1:n.529+99G>C
NM_005097.4:c.673+99G>C MANE Select	NP_005088.1:n.673+99G>C
NM_001308275.2:c.673+99G>C	NP_001295204.1:n.673+99G>C
NM_001308276.2:c.529+99G>C	NP_001295205.1:n.529+99G>C
NR_131777.2:n.810+99G>C