Canonical Allele Identifier: CA377623981

Gene: LGI1

Linked Data

• gnomAD v4: 10-93793212-T-C
• MyVariant Identifiers: chr10:g.95552969T>C (hg19) ; chr10:g.93793212T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793212T>C , CM000672.2:g.93793212T>C	GRCh38
NC_000010.10:g.95552969T>C , CM000672.1:g.95552969T>C	GRCh37
NC_000010.9:g.95542959T>C	NCBI36
NG_011832.1:g.40404T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.700T>C MANE Select	ENSP00000360472.4:p.Tyr234His
ENST00000485458.3:n.4676T>C
ENST00000635953.1:c.700T>C	ENSP00000490058.1:p.Tyr234His
ENST00000636155.1:c.700T>C	ENSP00000490355.1:p.Tyr234His
ENST00000636232.1:c.*486T>C	ENSP00000490325.1:n.*486T>C
ENST00000636754.1:c.*542T>C	ENSP00000489781.1:n.*542T>C
ENST00000636946.1:c.*869T>C	ENSP00000490654.1:n.*869T>C
ENST00000637037.1:c.*290T>C	ENSP00000490860.1:n.*290T>C
ENST00000637347.1:n.561T>C
ENST00000637611.1:c.*256T>C	ENSP00000489682.1:n.*256T>C
ENST00000637689.1:c.-672T>C	ENSP00000490496.1:n.-672T>C
ENST00000637925.1:c.*295T>C	ENSP00000489763.1:n.*295T>C
ENST00000638049.1:c.*458T>C	ENSP00000490597.1:n.*458T>C
ENST00000676175.1:n.2439T>C
ENST00000371413.4:c.700T>C	ENSP00000360467.3:p.Tyr234His
ENST00000371418.8:c.700T>C	ENSP00000360472.4:p.Tyr234His
ENST00000626307.1:n.4615T>C
ENST00000626946.1:n.370T>C
ENST00000627420.2:c.*409T>C	ENSP00000487116.1:n.*409T>C
ENST00000629035.2:c.628T>C	ENSP00000486908.1:p.Tyr210His
ENST00000630047.2:c.556T>C	ENSP00000485917.1:p.Tyr186His
ENST00000630412.1:n.488T>C
ENST00000630487.2:c.*490T>C	ENSP00000486859.1:n.*490T>C
NM_001308275.1:c.700T>C	NP_001295204.1:p.Tyr234His
NM_001308276.1:c.556T>C	NP_001295205.1:p.Tyr186His
NM_005097.2:c.700T>C	NP_005088.1:p.Tyr234His
NM_005097.3:c.700T>C	NP_005088.1:p.Tyr234His
NR_131777.1:n.964T>C
XM_017016911.2:c.700T>C	XP_016872400.1:p.Tyr234His
XM_017016912.2:c.556T>C	XP_016872401.1:p.Tyr186His
NM_005097.4:c.700T>C MANE Select	NP_005088.1:p.Tyr234His
NM_001308275.2:c.700T>C	NP_001295204.1:p.Tyr234His
NM_001308276.2:c.556T>C	NP_001295205.1:p.Tyr186His
NR_131777.2:n.837T>C