Canonical Allele Identifier: CA470800135

Gene: LGI1

Linked Data

• gnomAD v4: 10-93793310-C-T
• MyVariant Identifiers: chr10:g.95553067C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793310C>T , CM000672.2:g.93793310C>T	GRCh38
NC_000010.10:g.95553067C>T , CM000672.1:g.95553067C>T	GRCh37
NC_000010.9:g.95543057C>T	NCBI36
NG_011832.1:g.40502C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.798C>T MANE Select	ENSP00000360472.4:p.Asp266=
ENST00000485458.3:n.4774C>T
ENST00000635953.1:c.798C>T	ENSP00000490058.1:p.Asp266=
ENST00000636155.1:c.798C>T	ENSP00000490355.1:p.Asp266=
ENST00000636232.1:c.*584C>T	ENSP00000490325.1:n.*584C>T
ENST00000636754.1:c.*640C>T	ENSP00000489781.1:n.*640C>T
ENST00000636946.1:c.*967C>T	ENSP00000490654.1:n.*967C>T
ENST00000637037.1:c.*388C>T	ENSP00000490860.1:n.*388C>T
ENST00000637347.1:n.659C>T
ENST00000637611.1:c.*354C>T	ENSP00000489682.1:n.*354C>T
ENST00000637689.1:c.-574C>T	ENSP00000490496.1:n.-574C>T
ENST00000637925.1:c.*393C>T	ENSP00000489763.1:n.*393C>T
ENST00000638049.1:c.*556C>T	ENSP00000490597.1:n.*556C>T
ENST00000676175.1:n.2537C>T
ENST00000371413.4:c.798C>T	ENSP00000360467.3:p.Asp266=
ENST00000371418.8:c.798C>T	ENSP00000360472.4:p.Asp266=
ENST00000626307.1:n.4713C>T
ENST00000626946.1:n.468C>T
ENST00000627420.2:c.*507C>T	ENSP00000487116.1:n.*507C>T
ENST00000629035.2:c.726C>T	ENSP00000486908.1:p.Asp242=
ENST00000630047.2:c.654C>T	ENSP00000485917.1:p.Asp218=
ENST00000630487.2:c.*588C>T	ENSP00000486859.1:n.*588C>T
NM_001308275.1:c.798C>T	NP_001295204.1:p.Asp266=
NM_001308276.1:c.654C>T	NP_001295205.1:p.Asp218=
NM_005097.2:c.798C>T	NP_005088.1:p.Asp266=
NM_005097.3:c.798C>T	NP_005088.1:p.Asp266=
NR_131777.1:n.1062C>T
XM_017016911.2:c.798C>T	XP_016872400.1:p.Asp266=
XM_017016912.2:c.654C>T	XP_016872401.1:p.Asp218=
NM_005097.4:c.798C>T MANE Select	NP_005088.1:p.Asp266=
NM_001308275.2:c.798C>T	NP_001295204.1:p.Asp266=
NM_001308276.2:c.654C>T	NP_001295205.1:p.Asp218=
NR_131777.2:n.935C>T