Canonical Allele Identifier: CA470800080

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552965G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793208G>T , CM000672.2:g.93793208G>T	GRCh38
NC_000010.10:g.95552965G>T , CM000672.1:g.95552965G>T	GRCh37
NC_000010.9:g.95542955G>T	NCBI36
NG_011832.1:g.40400G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.696G>T MANE Select	ENSP00000360472.4:p.Leu232=
ENST00000485458.3:n.4672G>T
ENST00000635953.1:c.696G>T	ENSP00000490058.1:p.Leu232=
ENST00000636155.1:c.696G>T	ENSP00000490355.1:p.Leu232=
ENST00000636232.1:c.*482G>T	ENSP00000490325.1:n.*482G>T
ENST00000636754.1:c.*538G>T	ENSP00000489781.1:n.*538G>T
ENST00000636946.1:c.*865G>T	ENSP00000490654.1:n.*865G>T
ENST00000637037.1:c.*286G>T	ENSP00000490860.1:n.*286G>T
ENST00000637347.1:n.557G>T
ENST00000637611.1:c.*252G>T	ENSP00000489682.1:n.*252G>T
ENST00000637689.1:c.-676G>T	ENSP00000490496.1:n.-676G>T
ENST00000637925.1:c.*291G>T	ENSP00000489763.1:n.*291G>T
ENST00000638049.1:c.*454G>T	ENSP00000490597.1:n.*454G>T
ENST00000676175.1:n.2435G>T
ENST00000371413.4:c.696G>T	ENSP00000360467.3:p.Leu232=
ENST00000371418.8:c.696G>T	ENSP00000360472.4:p.Leu232=
ENST00000626307.1:n.4611G>T
ENST00000626946.1:n.366G>T
ENST00000627420.2:c.*405G>T	ENSP00000487116.1:n.*405G>T
ENST00000629035.2:c.624G>T	ENSP00000486908.1:p.Leu208=
ENST00000630047.2:c.552G>T	ENSP00000485917.1:p.Leu184=
ENST00000630412.1:n.484G>T
ENST00000630487.2:c.*486G>T	ENSP00000486859.1:n.*486G>T
NM_001308275.1:c.696G>T	NP_001295204.1:p.Leu232=
NM_001308276.1:c.552G>T	NP_001295205.1:p.Leu184=
NM_005097.2:c.696G>T	NP_005088.1:p.Leu232=
NM_005097.3:c.696G>T	NP_005088.1:p.Leu232=
NR_131777.1:n.960G>T
XM_017016911.2:c.696G>T	XP_016872400.1:p.Leu232=
XM_017016912.2:c.552G>T	XP_016872401.1:p.Leu184=
NM_005097.4:c.696G>T MANE Select	NP_005088.1:p.Leu232=
NM_001308275.2:c.696G>T	NP_001295204.1:p.Leu232=
NM_001308276.2:c.552G>T	NP_001295205.1:p.Leu184=
NR_131777.2:n.833G>T