Canonical Allele Identifier: CA377627228

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556923T>A (hg19) ; chr10:g.93797166T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797166T>A , CM000672.2:g.93797166T>A	GRCh38
NC_000010.10:g.95556923T>A , CM000672.1:g.95556923T>A	GRCh37
NC_000010.9:g.95546913T>A	NCBI36
NG_011832.1:g.44358T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1037T>A MANE Select	ENSP00000360472.4:p.Phe346Tyr
ENST00000485458.3:n.5013T>A
ENST00000635804.1:n.471T>A
ENST00000635953.1:c.*459T>A	ENSP00000490058.1:n.*459T>A
ENST00000636155.1:c.838+3816T>A	ENSP00000490355.1:n.838+3816T>A
ENST00000636232.1:c.*823T>A	ENSP00000490325.1:n.*823T>A
ENST00000636754.1:c.*879T>A	ENSP00000489781.1:n.*879T>A
ENST00000636946.1:c.*1008-583T>A	ENSP00000490654.1:n.*1008-583T>A
ENST00000637037.1:c.*627T>A	ENSP00000490860.1:n.*627T>A
ENST00000637347.1:n.898T>A
ENST00000637611.1:c.*593T>A	ENSP00000489682.1:n.*593T>A
ENST00000637689.1:c.-335T>A	ENSP00000490496.1:n.-335T>A
ENST00000637925.1:c.*632T>A	ENSP00000489763.1:n.*632T>A
ENST00000638049.1:c.*795T>A	ENSP00000490597.1:n.*795T>A
ENST00000676175.1:n.2776T>A
ENST00000371413.4:c.839-583T>A	ENSP00000360467.3:n.839-583T>A
ENST00000371418.8:c.1037T>A	ENSP00000360472.4:p.Phe346Tyr
ENST00000626307.1:n.4952T>A
ENST00000627420.2:c.*746T>A	ENSP00000487116.1:n.*746T>A
ENST00000629035.2:c.965T>A	ENSP00000486908.1:p.Phe322Tyr
ENST00000630047.2:c.893T>A	ENSP00000485917.1:p.Phe298Tyr
NM_001308275.1:c.839-583T>A	NP_001295204.1:n.839-583T>A
NM_001308276.1:c.893T>A	NP_001295205.1:p.Phe298Tyr
NM_005097.2:c.1037T>A	NP_005088.1:p.Phe346Tyr
NM_005097.3:c.1037T>A	NP_005088.1:p.Phe346Tyr
NR_131777.1:n.1301T>A
XM_017016912.2:c.695-583T>A	XP_016872401.1:n.695-583T>A
NM_005097.4:c.1037T>A MANE Select	NP_005088.1:p.Phe346Tyr
NM_001308275.2:c.839-583T>A	NP_001295204.1:n.839-583T>A
NM_001308276.2:c.893T>A	NP_001295205.1:p.Phe298Tyr
NR_131777.2:n.1174T>A