Canonical Allele Identifier: CA377622185

Gene: LGI1

Linked Data

• ClinVar Variation Id: 523479
• ClinVar RCV Id: RCV000626875
• dbSNP Id: rs1554906737
• MyVariant Identifiers: chr10:g.95549894A>T (hg19) ; chr10:g.93790137A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93790137A>T , CM000672.2:g.93790137A>T	GRCh38
NC_000010.10:g.95549894A>T , CM000672.1:g.95549894A>T	GRCh37
NC_000010.9:g.95539884A>T	NCBI36
NG_011832.1:g.37329A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.470A>T MANE Select	ENSP00000360472.4:p.Asp157Val
ENST00000485458.3:n.4446A>T
ENST00000635953.1:c.470A>T	ENSP00000490058.1:p.Asp157Val
ENST00000636155.1:c.470A>T	ENSP00000490355.1:p.Asp157Val
ENST00000636232.1:c.*256A>T	ENSP00000490325.1:n.*256A>T
ENST00000636754.1:c.*260A>T	ENSP00000489781.1:n.*260A>T
ENST00000636946.1:c.*639A>T	ENSP00000490654.1:n.*639A>T
ENST00000637037.1:c.*60A>T	ENSP00000490860.1:n.*60A>T
ENST00000637347.1:n.331A>T
ENST00000637611.1:c.470A>T	ENSP00000489682.1:p.Asp157Val
ENST00000637689.1:c.-902A>T	ENSP00000490496.1:n.-902A>T
ENST00000637925.1:c.*65A>T	ENSP00000489763.1:n.*65A>T
ENST00000638049.1:c.*228A>T	ENSP00000490597.1:n.*228A>T
ENST00000676175.1:n.2209A>T
ENST00000371413.4:c.470A>T	ENSP00000360467.3:p.Asp157Val
ENST00000371418.8:c.470A>T	ENSP00000360472.4:p.Asp157Val
ENST00000485458.2:n.385A>T
ENST00000626307.1:n.1813A>T
ENST00000627420.2:c.*116A>T	ENSP00000487116.1:n.*116A>T
ENST00000629035.2:c.398A>T	ENSP00000486908.1:p.Asp133Val
ENST00000630047.2:c.326A>T	ENSP00000485917.1:p.Asp109Val
ENST00000630184.2:c.470A>T	ENSP00000486607.1:p.Asp157Val
ENST00000630412.1:n.258A>T
ENST00000630487.2:c.*260A>T	ENSP00000486859.1:n.*260A>T
NM_001308275.1:c.470A>T	NP_001295204.1:p.Asp157Val
NM_001308276.1:c.326A>T	NP_001295205.1:p.Asp109Val
NM_005097.2:c.470A>T	NP_005088.1:p.Asp157Val
NM_005097.3:c.470A>T	NP_005088.1:p.Asp157Val
NR_131777.1:n.671A>T
XM_017016911.2:c.470A>T	XP_016872400.1:p.Asp157Val
XM_017016912.2:c.326A>T	XP_016872401.1:p.Asp109Val
NM_005097.4:c.470A>T MANE Select	NP_005088.1:p.Asp157Val
NM_001308275.2:c.470A>T	NP_001295204.1:p.Asp157Val
NM_001308276.2:c.326A>T	NP_001295205.1:p.Asp109Val
NR_131777.2:n.544A>T