Canonical Allele Identifier: CA377624576

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553092T>C (hg19) ; chr10:g.93793335T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793335T>C , CM000672.2:g.93793335T>C	GRCh38
NC_000010.10:g.95553092T>C , CM000672.1:g.95553092T>C	GRCh37
NC_000010.9:g.95543082T>C	NCBI36
NG_011832.1:g.40527T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.823T>C MANE Select	ENSP00000360472.4:p.Tyr275His
ENST00000485458.3:n.4799T>C
ENST00000635953.1:c.823T>C	ENSP00000490058.1:p.Tyr275His
ENST00000636155.1:c.823T>C	ENSP00000490355.1:p.Tyr275His
ENST00000636232.1:c.*609T>C	ENSP00000490325.1:n.*609T>C
ENST00000636754.1:c.*665T>C	ENSP00000489781.1:n.*665T>C
ENST00000636946.1:c.*992T>C	ENSP00000490654.1:n.*992T>C
ENST00000637037.1:c.*413T>C	ENSP00000490860.1:n.*413T>C
ENST00000637347.1:n.684T>C
ENST00000637611.1:c.*379T>C	ENSP00000489682.1:n.*379T>C
ENST00000637689.1:c.-549T>C	ENSP00000490496.1:n.-549T>C
ENST00000637925.1:c.*418T>C	ENSP00000489763.1:n.*418T>C
ENST00000638049.1:c.*581T>C	ENSP00000490597.1:n.*581T>C
ENST00000676175.1:n.2562T>C
ENST00000371413.4:c.823T>C	ENSP00000360467.3:p.Tyr275His
ENST00000371418.8:c.823T>C	ENSP00000360472.4:p.Tyr275His
ENST00000626307.1:n.4738T>C
ENST00000626946.1:n.493T>C
ENST00000627420.2:c.*532T>C	ENSP00000487116.1:n.*532T>C
ENST00000629035.2:c.751T>C	ENSP00000486908.1:p.Tyr251His
ENST00000630047.2:c.679T>C	ENSP00000485917.1:p.Tyr227His
ENST00000630487.2:c.*613T>C	ENSP00000486859.1:n.*613T>C
NM_001308275.1:c.823T>C	NP_001295204.1:p.Tyr275His
NM_001308276.1:c.679T>C	NP_001295205.1:p.Tyr227His
NM_005097.2:c.823T>C	NP_005088.1:p.Tyr275His
NM_005097.3:c.823T>C	NP_005088.1:p.Tyr275His
NR_131777.1:n.1087T>C
XM_017016911.2:c.823T>C	XP_016872400.1:p.Tyr275His
XM_017016912.2:c.679T>C	XP_016872401.1:p.Tyr227His
NM_005097.4:c.823T>C MANE Select	NP_005088.1:p.Tyr275His
NM_001308275.2:c.823T>C	NP_001295204.1:p.Tyr275His
NM_001308276.2:c.679T>C	NP_001295205.1:p.Tyr227His
NR_131777.2:n.960T>C