Canonical Allele Identifier: CA2610220373

Gene: LGI1

Linked Data

• gnomAD v4: 10-93758921-AATGTGATTCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93758924_93758933del , CM000672.2:g.93758924_93758933del	GRCh38
NC_000010.10:g.95518681_95518690del , CM000672.1:g.95518681_95518690del	GRCh37
NC_000010.9:g.95508671_95508680del	NCBI36
NG_011832.1:g.6116_6125del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.287+93_287+102del MANE Select	ENSP00000360472.4:n.287+93_287+102del
ENST00000635953.1:c.287+93_287+102del	ENSP00000490058.1:n.287+93_287+102del
ENST00000636140.1:n.72+93_72+102del
ENST00000636155.1:c.287+93_287+102del	ENSP00000490355.1:n.287+93_287+102del
ENST00000636232.1:c.*73+93_*73+102del	ENSP00000490325.1:n.*73+93_*73+102del
ENST00000636683.1:n.42+93_42+102del
ENST00000636754.1:c.*77+93_*77+102del	ENSP00000489781.1:n.*77+93_*77+102del
ENST00000636946.1:c.*89_*98del	ENSP00000490654.1:n.*89_*98del
ENST00000637037.1:c.287+93_287+102del	ENSP00000490860.1:n.287+93_287+102del
ENST00000637347.1:n.148+236_148+245del
ENST00000637611.1:c.287+93_287+102del	ENSP00000489682.1:n.287+93_287+102del
ENST00000637689.1:c.-1085+93_-1085+102del	ENSP00000490496.1:n.-1085+93_-1085+102del
ENST00000637925.1:c.287+93_287+102del	ENSP00000489763.1:n.287+93_287+102del
ENST00000638049.1:c.*45+93_*45+102del	ENSP00000490597.1:n.*45+93_*45+102del
ENST00000371413.4:c.287+93_287+102del	ENSP00000360467.3:n.287+93_287+102del
ENST00000371418.8:c.287+93_287+102del	ENSP00000360472.4:n.287+93_287+102del
ENST00000627420.2:c.*77+93_*77+102del	ENSP00000487116.1:n.*77+93_*77+102del
ENST00000627699.1:c.*170_*179del	ENSP00000485868.1:n.*170_*179del
ENST00000629035.2:c.215+565_215+574del	ENSP00000486908.1:n.215+565_215+574del
ENST00000630047.2:c.287+93_287+102del	ENSP00000485917.1:n.287+93_287+102del
ENST00000630184.2:c.287+93_287+102del	ENSP00000486607.1:n.287+93_287+102del
ENST00000630487.2:c.*77+93_*77+102del	ENSP00000486859.1:n.*77+93_*77+102del
NM_001308275.1:c.287+93_287+102del	NP_001295204.1:n.287+93_287+102del
NM_001308276.1:c.287+93_287+102del	NP_001295205.1:n.287+93_287+102del
NM_005097.2:c.287+93_287+102del	NP_005088.1:n.287+93_287+102del
NM_005097.3:c.287+93_287+102del	NP_005088.1:n.287+93_287+102del
NR_131777.1:n.632+93_632+102del
XM_017016911.2:c.287+93_287+102del	XP_016872400.1:n.287+93_287+102del
XM_017016912.2:c.287+93_287+102del	XP_016872401.1:n.287+93_287+102del
XR_001747552.1:n.4944_4953del
XR_002957095.1:n.7072_7081del
XR_002957096.1:n.8284_8293del
NM_005097.4:c.287+93_287+102del MANE Select	NP_005088.1:n.287+93_287+102del
NM_001308275.2:c.287+93_287+102del	NP_001295204.1:n.287+93_287+102del
NM_001308276.2:c.287+93_287+102del	NP_001295205.1:n.287+93_287+102del
NR_131777.2:n.505+93_505+102del