Canonical Allele Identifier: CA377623967

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552966C>A (hg19) ; chr10:g.93793209C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793209C>A , CM000672.2:g.93793209C>A	GRCh38
NC_000010.10:g.95552966C>A , CM000672.1:g.95552966C>A	GRCh37
NC_000010.9:g.95542956C>A	NCBI36
NG_011832.1:g.40401C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.697C>A MANE Select	ENSP00000360472.4:p.Pro233Thr
ENST00000485458.3:n.4673C>A
ENST00000635953.1:c.697C>A	ENSP00000490058.1:p.Pro233Thr
ENST00000636155.1:c.697C>A	ENSP00000490355.1:p.Pro233Thr
ENST00000636232.1:c.*483C>A	ENSP00000490325.1:n.*483C>A
ENST00000636754.1:c.*539C>A	ENSP00000489781.1:n.*539C>A
ENST00000636946.1:c.*866C>A	ENSP00000490654.1:n.*866C>A
ENST00000637037.1:c.*287C>A	ENSP00000490860.1:n.*287C>A
ENST00000637347.1:n.558C>A
ENST00000637611.1:c.*253C>A	ENSP00000489682.1:n.*253C>A
ENST00000637689.1:c.-675C>A	ENSP00000490496.1:n.-675C>A
ENST00000637925.1:c.*292C>A	ENSP00000489763.1:n.*292C>A
ENST00000638049.1:c.*455C>A	ENSP00000490597.1:n.*455C>A
ENST00000676175.1:n.2436C>A
ENST00000371413.4:c.697C>A	ENSP00000360467.3:p.Pro233Thr
ENST00000371418.8:c.697C>A	ENSP00000360472.4:p.Pro233Thr
ENST00000626307.1:n.4612C>A
ENST00000626946.1:n.367C>A
ENST00000627420.2:c.*406C>A	ENSP00000487116.1:n.*406C>A
ENST00000629035.2:c.625C>A	ENSP00000486908.1:p.Pro209Thr
ENST00000630047.2:c.553C>A	ENSP00000485917.1:p.Pro185Thr
ENST00000630412.1:n.485C>A
ENST00000630487.2:c.*487C>A	ENSP00000486859.1:n.*487C>A
NM_001308275.1:c.697C>A	NP_001295204.1:p.Pro233Thr
NM_001308276.1:c.553C>A	NP_001295205.1:p.Pro185Thr
NM_005097.2:c.697C>A	NP_005088.1:p.Pro233Thr
NM_005097.3:c.697C>A	NP_005088.1:p.Pro233Thr
NR_131777.1:n.961C>A
XM_017016911.2:c.697C>A	XP_016872400.1:p.Pro233Thr
XM_017016912.2:c.553C>A	XP_016872401.1:p.Pro185Thr
NM_005097.4:c.697C>A MANE Select	NP_005088.1:p.Pro233Thr
NM_001308275.2:c.697C>A	NP_001295204.1:p.Pro233Thr
NM_001308276.2:c.553C>A	NP_001295205.1:p.Pro185Thr
NR_131777.2:n.834C>A