Canonical Allele Identifier: CA377624599

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553095G>T (hg19) ; chr10:g.93793338G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793338G>T , CM000672.2:g.93793338G>T	GRCh38
NC_000010.10:g.95553095G>T , CM000672.1:g.95553095G>T	GRCh37
NC_000010.9:g.95543085G>T	NCBI36
NG_011832.1:g.40530G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.826G>T MANE Select	ENSP00000360472.4:p.Asp276Tyr
ENST00000485458.3:n.4802G>T
ENST00000635953.1:c.826G>T	ENSP00000490058.1:p.Asp276Tyr
ENST00000636155.1:c.826G>T	ENSP00000490355.1:p.Asp276Tyr
ENST00000636232.1:c.*612G>T	ENSP00000490325.1:n.*612G>T
ENST00000636754.1:c.*668G>T	ENSP00000489781.1:n.*668G>T
ENST00000636946.1:c.*995G>T	ENSP00000490654.1:n.*995G>T
ENST00000637037.1:c.*416G>T	ENSP00000490860.1:n.*416G>T
ENST00000637347.1:n.687G>T
ENST00000637611.1:c.*382G>T	ENSP00000489682.1:n.*382G>T
ENST00000637689.1:c.-546G>T	ENSP00000490496.1:n.-546G>T
ENST00000637925.1:c.*421G>T	ENSP00000489763.1:n.*421G>T
ENST00000638049.1:c.*584G>T	ENSP00000490597.1:n.*584G>T
ENST00000676175.1:n.2565G>T
ENST00000371413.4:c.826G>T	ENSP00000360467.3:p.Asp276Tyr
ENST00000371418.8:c.826G>T	ENSP00000360472.4:p.Asp276Tyr
ENST00000626307.1:n.4741G>T
ENST00000626946.1:n.496G>T
ENST00000627420.2:c.*535G>T	ENSP00000487116.1:n.*535G>T
ENST00000629035.2:c.754G>T	ENSP00000486908.1:p.Asp252Tyr
ENST00000630047.2:c.682G>T	ENSP00000485917.1:p.Asp228Tyr
ENST00000630487.2:c.*616G>T	ENSP00000486859.1:n.*616G>T
NM_001308275.1:c.826G>T	NP_001295204.1:p.Asp276Tyr
NM_001308276.1:c.682G>T	NP_001295205.1:p.Asp228Tyr
NM_005097.2:c.826G>T	NP_005088.1:p.Asp276Tyr
NM_005097.3:c.826G>T	NP_005088.1:p.Asp276Tyr
NR_131777.1:n.1090G>T
XM_017016911.2:c.826G>T	XP_016872400.1:p.Asp276Tyr
XM_017016912.2:c.682G>T	XP_016872401.1:p.Asp228Tyr
NM_005097.4:c.826G>T MANE Select	NP_005088.1:p.Asp276Tyr
NM_001308275.2:c.826G>T	NP_001295204.1:p.Asp276Tyr
NM_001308276.2:c.682G>T	NP_001295205.1:p.Asp228Tyr
NR_131777.2:n.963G>T