Canonical Allele Identifier: CA1928770991
Gene: LGI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93793333A= , CM000672.2:g.93793333A= GRCh38
NC_000010.10:g.95553090A= , CM000672.1:g.95553090A= GRCh37
NC_000010.9:g.95543080A= NCBI36
NG_011832.1:g.40525A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371418.9:c.821A= MANE Select ENSP00000360472.4:p.Asn274=
ENST00000485458.3:n.4797A=
ENST00000635953.1:c.821A= ENSP00000490058.1:p.Asn274=
ENST00000636155.1:c.821A= ENSP00000490355.1:p.Asn274=
ENST00000636232.1:c.*607A= ENSP00000490325.1:n.*607A=
ENST00000636754.1:c.*663A= ENSP00000489781.1:n.*663A=
ENST00000636946.1:c.*990A= ENSP00000490654.1:n.*990A=
ENST00000637037.1:c.*411A= ENSP00000490860.1:n.*411A=
ENST00000637347.1:n.682A=
ENST00000637611.1:c.*377A= ENSP00000489682.1:n.*377A=
ENST00000637689.1:c.-551A= ENSP00000490496.1:n.-551A=
ENST00000637925.1:c.*416A= ENSP00000489763.1:n.*416A=
ENST00000638049.1:c.*579A= ENSP00000490597.1:n.*579A=
ENST00000676175.1:n.2560A=
ENST00000371413.4:c.821A= ENSP00000360467.3:p.Asn274=
ENST00000371418.8:c.821A= ENSP00000360472.4:p.Asn274=
ENST00000626307.1:n.4736A=
ENST00000626946.1:n.491A=
ENST00000627420.2:c.*530A= ENSP00000487116.1:n.*530A=
ENST00000629035.2:c.749A= ENSP00000486908.1:p.Asn250=
ENST00000630047.2:c.677A= ENSP00000485917.1:p.Asn226=
ENST00000630487.2:c.*611A= ENSP00000486859.1:n.*611A=
NM_001308275.1:c.821A= NP_001295204.1:p.Asn274=
NM_001308276.1:c.677A= NP_001295205.1:p.Asn226=
NM_005097.2:c.821A= NP_005088.1:p.Asn274=
NM_005097.3:c.821A= NP_005088.1:p.Asn274=
NR_131777.1:n.1085A=
XM_017016911.2:c.821A= XP_016872400.1:p.Asn274=
XM_017016912.2:c.677A= XP_016872401.1:p.Asn226=
NM_005097.4:c.821A= MANE Select NP_005088.1:p.Asn274=
NM_001308275.2:c.821A= NP_001295204.1:p.Asn274=
NM_001308276.2:c.677A= NP_001295205.1:p.Asn226=
NR_131777.2:n.958A=