Canonical Allele Identifier: CA377623937

Gene: LGI1

Linked Data

• dbSNP Id: rs2059950875
• MyVariant Identifiers: chr10:g.95552958A>C (hg19) ; chr10:g.93793201A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793201A>C , CM000672.2:g.93793201A>C	GRCh38
NC_000010.10:g.95552958A>C , CM000672.1:g.95552958A>C	GRCh37
NC_000010.9:g.95542948A>C	NCBI36
NG_011832.1:g.40393A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.689A>C MANE Select	ENSP00000360472.4:p.Gln230Pro
ENST00000485458.3:n.4665A>C
ENST00000635953.1:c.689A>C	ENSP00000490058.1:p.Gln230Pro
ENST00000636155.1:c.689A>C	ENSP00000490355.1:p.Gln230Pro
ENST00000636232.1:c.*475A>C	ENSP00000490325.1:n.*475A>C
ENST00000636754.1:c.*531A>C	ENSP00000489781.1:n.*531A>C
ENST00000636946.1:c.*858A>C	ENSP00000490654.1:n.*858A>C
ENST00000637037.1:c.*279A>C	ENSP00000490860.1:n.*279A>C
ENST00000637347.1:n.550A>C
ENST00000637611.1:c.*245A>C	ENSP00000489682.1:n.*245A>C
ENST00000637689.1:c.-683A>C	ENSP00000490496.1:n.-683A>C
ENST00000637925.1:c.*284A>C	ENSP00000489763.1:n.*284A>C
ENST00000638049.1:c.*447A>C	ENSP00000490597.1:n.*447A>C
ENST00000676175.1:n.2428A>C
ENST00000371413.4:c.689A>C	ENSP00000360467.3:p.Gln230Pro
ENST00000371418.8:c.689A>C	ENSP00000360472.4:p.Gln230Pro
ENST00000626307.1:n.4604A>C
ENST00000626946.1:n.359A>C
ENST00000627420.2:c.*398A>C	ENSP00000487116.1:n.*398A>C
ENST00000629035.2:c.617A>C	ENSP00000486908.1:p.Gln206Pro
ENST00000630047.2:c.545A>C	ENSP00000485917.1:p.Gln182Pro
ENST00000630412.1:n.477A>C
ENST00000630487.2:c.*479A>C	ENSP00000486859.1:n.*479A>C
NM_001308275.1:c.689A>C	NP_001295204.1:p.Gln230Pro
NM_001308276.1:c.545A>C	NP_001295205.1:p.Gln182Pro
NM_005097.2:c.689A>C	NP_005088.1:p.Gln230Pro
NM_005097.3:c.689A>C	NP_005088.1:p.Gln230Pro
NR_131777.1:n.953A>C
XM_017016911.2:c.689A>C	XP_016872400.1:p.Gln230Pro
XM_017016912.2:c.545A>C	XP_016872401.1:p.Gln182Pro
NM_005097.4:c.689A>C MANE Select	NP_005088.1:p.Gln230Pro
NM_001308275.2:c.689A>C	NP_001295204.1:p.Gln230Pro
NM_001308276.2:c.545A>C	NP_001295205.1:p.Gln182Pro
NR_131777.2:n.826A>C