Canonical Allele Identifier: CA2333512004
Gene: LGI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35126755T= , CM000681.2:g.35126755T= GRCh38
NC_000019.9:g.35617659T= , CM000681.1:g.35617659T= GRCh37
NC_000019.8:g.40309499T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310123.8:c.814A= MANE Select ENSP00000312273.3:p.Lys272=
ENST00000310123.7:c.814A= ENSP00000312273.3:p.Lys272=
ENST00000392225.7:c.891A= ENSP00000376059.3:p.Ala297=
ENST00000493050.5:n.873A=
ENST00000587780.5:c.549A=
ENST00000591840.5:n.420-1889A=
ENST00000593248.5:n.1022A=
NM_139284.2:c.814A= NP_644813.1:p.Lys272=
XM_011526594.1:c.814A= XP_011524896.1:p.Lys272=
XM_011526595.1:c.298A= XP_011524897.1:p.Lys100=
XM_011526595.2:c.298A= XP_011524897.1:p.Lys100=
XM_017026428.1:c.298A= XP_016881917.1:p.Lys100=
XM_017026429.1:c.298A= XP_016881918.1:p.Lys100=
XM_017026430.2:c.298A= XP_016881919.1:p.Lys100=
NM_139284.3:c.814A= MANE Select NP_644813.1:p.Lys272=