Canonical Allele Identifier: CA377624662

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553105C>T (hg19) ; chr10:g.93793348C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793348C>T , CM000672.2:g.93793348C>T	GRCh38
NC_000010.10:g.95553105C>T , CM000672.1:g.95553105C>T	GRCh37
NC_000010.9:g.95543095C>T	NCBI36
NG_011832.1:g.40540C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.836C>T MANE Select	ENSP00000360472.4:p.Thr279Ile
ENST00000485458.3:n.4812C>T
ENST00000635953.1:c.836C>T	ENSP00000490058.1:p.Thr279Ile
ENST00000636155.1:c.836C>T	ENSP00000490355.1:p.Thr279Ile
ENST00000636232.1:c.*622C>T	ENSP00000490325.1:n.*622C>T
ENST00000636754.1:c.*678C>T	ENSP00000489781.1:n.*678C>T
ENST00000636946.1:c.*1005C>T	ENSP00000490654.1:n.*1005C>T
ENST00000637037.1:c.*426C>T	ENSP00000490860.1:n.*426C>T
ENST00000637347.1:n.697C>T
ENST00000637611.1:c.*392C>T	ENSP00000489682.1:n.*392C>T
ENST00000637689.1:c.-536C>T	ENSP00000490496.1:n.-536C>T
ENST00000637925.1:c.*431C>T	ENSP00000489763.1:n.*431C>T
ENST00000638049.1:c.*594C>T	ENSP00000490597.1:n.*594C>T
ENST00000676175.1:n.2575C>T
ENST00000371413.4:c.836C>T	ENSP00000360467.3:p.Thr279Ile
ENST00000371418.8:c.836C>T	ENSP00000360472.4:p.Thr279Ile
ENST00000626307.1:n.4751C>T
ENST00000626946.1:n.506C>T
ENST00000627420.2:c.*545C>T	ENSP00000487116.1:n.*545C>T
ENST00000629035.2:c.764C>T	ENSP00000486908.1:p.Thr255Ile
ENST00000630047.2:c.692C>T	ENSP00000485917.1:p.Thr231Ile
NM_001308275.1:c.836C>T	NP_001295204.1:p.Thr279Ile
NM_001308276.1:c.692C>T	NP_001295205.1:p.Thr231Ile
NM_005097.2:c.836C>T	NP_005088.1:p.Thr279Ile
NM_005097.3:c.836C>T	NP_005088.1:p.Thr279Ile
NR_131777.1:n.1100C>T
XM_017016911.2:c.836C>T	XP_016872400.1:p.Thr279Ile
XM_017016912.2:c.692C>T	XP_016872401.1:p.Thr231Ile
NM_005097.4:c.836C>T MANE Select	NP_005088.1:p.Thr279Ile
NM_001308275.2:c.836C>T	NP_001295204.1:p.Thr279Ile
NM_001308276.2:c.692C>T	NP_001295205.1:p.Thr231Ile
NR_131777.2:n.973C>T