Canonical Allele Identifier: CA595280134

Gene: LGI1

Linked Data

• dbSNP Id: rs1564837135
• gnomAD v2: 10-95518611-CTA-C
• gnomAD v4: 10-93758854-CTA-C
• MyVariant Identifiers: chr10:g.95518612_95518613del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93758856_93758857del , CM000672.2:g.93758856_93758857del	GRCh38
NC_000010.10:g.95518613_95518614del , CM000672.1:g.95518613_95518614del	GRCh37
NC_000010.9:g.95508603_95508604del	NCBI36
NG_011832.1:g.6048_6049del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.287+25_287+26del MANE Select	ENSP00000360472.4:n.287+25_287+26del
ENST00000635953.1:c.287+25_287+26del	ENSP00000490058.1:n.287+25_287+26del
ENST00000636140.1:n.72+25_72+26del
ENST00000636155.1:c.287+25_287+26del	ENSP00000490355.1:n.287+25_287+26del
ENST00000636232.1:c.*73+25_*73+26del	ENSP00000490325.1:n.*73+25_*73+26del
ENST00000636683.1:n.42+25_42+26del
ENST00000636754.1:c.*77+25_*77+26del	ENSP00000489781.1:n.*77+25_*77+26del
ENST00000636946.1:c.*21_*22del	ENSP00000490654.1:n.*21_*22del
ENST00000637037.1:c.287+25_287+26del	ENSP00000490860.1:n.287+25_287+26del
ENST00000637347.1:n.148+168_148+169del
ENST00000637611.1:c.287+25_287+26del	ENSP00000489682.1:n.287+25_287+26del
ENST00000637689.1:c.-1085+25_-1085+26del	ENSP00000490496.1:n.-1085+25_-1085+26del
ENST00000637925.1:c.287+25_287+26del	ENSP00000489763.1:n.287+25_287+26del
ENST00000638049.1:c.*45+25_*45+26del	ENSP00000490597.1:n.*45+25_*45+26del
ENST00000371413.4:c.287+25_287+26del	ENSP00000360467.3:n.287+25_287+26del
ENST00000371418.8:c.287+25_287+26del	ENSP00000360472.4:n.287+25_287+26del
ENST00000478763.2:c.*21_*22del	ENSP00000486517.1:n.*21_*22del
ENST00000627420.2:c.*77+25_*77+26del	ENSP00000487116.1:n.*77+25_*77+26del
ENST00000627699.1:c.*102_*103del	ENSP00000485868.1:n.*102_*103del
ENST00000629035.2:c.215+497_215+498del	ENSP00000486908.1:n.215+497_215+498del
ENST00000630047.2:c.287+25_287+26del	ENSP00000485917.1:n.287+25_287+26del
ENST00000630184.2:c.287+25_287+26del	ENSP00000486607.1:n.287+25_287+26del
ENST00000630487.2:c.*77+25_*77+26del	ENSP00000486859.1:n.*77+25_*77+26del
NM_001308275.1:c.287+25_287+26del	NP_001295204.1:n.287+25_287+26del
NM_001308276.1:c.287+25_287+26del	NP_001295205.1:n.287+25_287+26del
NM_005097.2:c.287+25_287+26del	NP_005088.1:n.287+25_287+26del
NM_005097.3:c.287+25_287+26del	NP_005088.1:n.287+25_287+26del
NR_131777.1:n.632+25_632+26del
XM_017016911.2:c.287+25_287+26del	XP_016872400.1:n.287+25_287+26del
XM_017016912.2:c.287+25_287+26del	XP_016872401.1:n.287+25_287+26del
XR_001747552.1:n.5019_5020del
XR_002957095.1:n.7147_7148del
XR_002957096.1:n.8359_8360del
NM_005097.4:c.287+25_287+26del MANE Select	NP_005088.1:n.287+25_287+26del
NM_001308275.2:c.287+25_287+26del	NP_001295204.1:n.287+25_287+26del
NM_001308276.2:c.287+25_287+26del	NP_001295205.1:n.287+25_287+26del
NR_131777.2:n.505+25_505+26del