Canonical Allele Identifier: CA377624395

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553063G>T (hg19) ; chr10:g.93793306G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793306G>T , CM000672.2:g.93793306G>T	GRCh38
NC_000010.10:g.95553063G>T , CM000672.1:g.95553063G>T	GRCh37
NC_000010.9:g.95543053G>T	NCBI36
NG_011832.1:g.40498G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.794G>T MANE Select	ENSP00000360472.4:p.Trp265Leu
ENST00000485458.3:n.4770G>T
ENST00000635953.1:c.794G>T	ENSP00000490058.1:p.Trp265Leu
ENST00000636155.1:c.794G>T	ENSP00000490355.1:p.Trp265Leu
ENST00000636232.1:c.*580G>T	ENSP00000490325.1:n.*580G>T
ENST00000636754.1:c.*636G>T	ENSP00000489781.1:n.*636G>T
ENST00000636946.1:c.*963G>T	ENSP00000490654.1:n.*963G>T
ENST00000637037.1:c.*384G>T	ENSP00000490860.1:n.*384G>T
ENST00000637347.1:n.655G>T
ENST00000637611.1:c.*350G>T	ENSP00000489682.1:n.*350G>T
ENST00000637689.1:c.-578G>T	ENSP00000490496.1:n.-578G>T
ENST00000637925.1:c.*389G>T	ENSP00000489763.1:n.*389G>T
ENST00000638049.1:c.*552G>T	ENSP00000490597.1:n.*552G>T
ENST00000676175.1:n.2533G>T
ENST00000371413.4:c.794G>T	ENSP00000360467.3:p.Trp265Leu
ENST00000371418.8:c.794G>T	ENSP00000360472.4:p.Trp265Leu
ENST00000626307.1:n.4709G>T
ENST00000626946.1:n.464G>T
ENST00000627420.2:c.*503G>T	ENSP00000487116.1:n.*503G>T
ENST00000629035.2:c.722G>T	ENSP00000486908.1:p.Trp241Leu
ENST00000630047.2:c.650G>T	ENSP00000485917.1:p.Trp217Leu
ENST00000630487.2:c.*584G>T	ENSP00000486859.1:n.*584G>T
NM_001308275.1:c.794G>T	NP_001295204.1:p.Trp265Leu
NM_001308276.1:c.650G>T	NP_001295205.1:p.Trp217Leu
NM_005097.2:c.794G>T	NP_005088.1:p.Trp265Leu
NM_005097.3:c.794G>T	NP_005088.1:p.Trp265Leu
NR_131777.1:n.1058G>T
XM_017016911.2:c.794G>T	XP_016872400.1:p.Trp265Leu
XM_017016912.2:c.650G>T	XP_016872401.1:p.Trp217Leu
NM_005097.4:c.794G>T MANE Select	NP_005088.1:p.Trp265Leu
NM_001308275.2:c.794G>T	NP_001295204.1:p.Trp265Leu
NM_001308276.2:c.650G>T	NP_001295205.1:p.Trp217Leu
NR_131777.2:n.931G>T