Canonical Allele Identifier: CA2333512006
Gene: LGI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35126760G= , CM000681.2:g.35126760G= GRCh38
NC_000019.9:g.35617664G= , CM000681.1:g.35617664G= GRCh37
NC_000019.8:g.40309504G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310123.8:c.809C= MANE Select ENSP00000312273.3:p.Ser270=
ENST00000310123.7:c.809C= ENSP00000312273.3:p.Ser270=
ENST00000392225.7:c.886C= ENSP00000376059.3:p.Pro296=
ENST00000493050.5:n.868C=
ENST00000587780.5:c.544C=
ENST00000591840.5:n.420-1894C=
ENST00000593248.5:n.1017C=
NM_139284.2:c.809C= NP_644813.1:p.Ser270=
XM_011526594.1:c.809C= XP_011524896.1:p.Ser270=
XM_011526595.1:c.293C= XP_011524897.1:p.Ser98=
XM_011526595.2:c.293C= XP_011524897.1:p.Ser98=
XM_017026428.1:c.293C= XP_016881917.1:p.Ser98=
XM_017026429.1:c.293C= XP_016881918.1:p.Ser98=
XM_017026430.2:c.293C= XP_016881919.1:p.Ser98=
NM_139284.3:c.809C= MANE Select NP_644813.1:p.Ser270=