Canonical Allele Identifier: CA377624508

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553080A>C (hg19) ; chr10:g.93793323A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793323A>C , CM000672.2:g.93793323A>C	GRCh38
NC_000010.10:g.95553080A>C , CM000672.1:g.95553080A>C	GRCh37
NC_000010.9:g.95543070A>C	NCBI36
NG_011832.1:g.40515A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.811A>C MANE Select	ENSP00000360472.4:p.Thr271Pro
ENST00000485458.3:n.4787A>C
ENST00000635953.1:c.811A>C	ENSP00000490058.1:p.Thr271Pro
ENST00000636155.1:c.811A>C	ENSP00000490355.1:p.Thr271Pro
ENST00000636232.1:c.*597A>C	ENSP00000490325.1:n.*597A>C
ENST00000636754.1:c.*653A>C	ENSP00000489781.1:n.*653A>C
ENST00000636946.1:c.*980A>C	ENSP00000490654.1:n.*980A>C
ENST00000637037.1:c.*401A>C	ENSP00000490860.1:n.*401A>C
ENST00000637347.1:n.672A>C
ENST00000637611.1:c.*367A>C	ENSP00000489682.1:n.*367A>C
ENST00000637689.1:c.-561A>C	ENSP00000490496.1:n.-561A>C
ENST00000637925.1:c.*406A>C	ENSP00000489763.1:n.*406A>C
ENST00000638049.1:c.*569A>C	ENSP00000490597.1:n.*569A>C
ENST00000676175.1:n.2550A>C
ENST00000371413.4:c.811A>C	ENSP00000360467.3:p.Thr271Pro
ENST00000371418.8:c.811A>C	ENSP00000360472.4:p.Thr271Pro
ENST00000626307.1:n.4726A>C
ENST00000626946.1:n.481A>C
ENST00000627420.2:c.*520A>C	ENSP00000487116.1:n.*520A>C
ENST00000629035.2:c.739A>C	ENSP00000486908.1:p.Thr247Pro
ENST00000630047.2:c.667A>C	ENSP00000485917.1:p.Thr223Pro
ENST00000630487.2:c.*601A>C	ENSP00000486859.1:n.*601A>C
NM_001308275.1:c.811A>C	NP_001295204.1:p.Thr271Pro
NM_001308276.1:c.667A>C	NP_001295205.1:p.Thr223Pro
NM_005097.2:c.811A>C	NP_005088.1:p.Thr271Pro
NM_005097.3:c.811A>C	NP_005088.1:p.Thr271Pro
NR_131777.1:n.1075A>C
XM_017016911.2:c.811A>C	XP_016872400.1:p.Thr271Pro
XM_017016912.2:c.667A>C	XP_016872401.1:p.Thr223Pro
NM_005097.4:c.811A>C MANE Select	NP_005088.1:p.Thr271Pro
NM_001308275.2:c.811A>C	NP_001295204.1:p.Thr271Pro
NM_001308276.2:c.667A>C	NP_001295205.1:p.Thr223Pro
NR_131777.2:n.948A>C