Canonical Allele Identifier: CA2814235753
Gene: LGI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35126756del , CM000681.2:g.35126756del GRCh38
NC_000019.9:g.35617660del , CM000681.1:g.35617660del GRCh37
NC_000019.8:g.40309500del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310123.8:c.813del MANE Select ENSP00000312273.3:p.Cys271Ter
ENST00000310123.7:c.813del ENSP00000312273.3:p.Cys271Ter
ENST00000392225.7:c.890del ENSP00000376059.3:p.Ala297GlufsTer?
ENST00000493050.5:n.872del
ENST00000587780.5:c.548del
ENST00000591840.5:n.420-1890del
ENST00000593248.5:n.1021del
NM_139284.2:c.813del NP_644813.1:p.Cys271Ter
XM_011526594.1:c.813del XP_011524896.1:p.Cys271Ter
XM_011526595.1:c.297del XP_011524897.1:p.Cys99Ter
XM_011526595.2:c.297del XP_011524897.1:p.Cys99Ter
XM_017026428.1:c.297del XP_016881917.1:p.Cys99Ter
XM_017026429.1:c.297del XP_016881918.1:p.Cys99Ter
XM_017026430.2:c.297del XP_016881919.1:p.Cys99Ter
NM_139284.3:c.813del MANE Select NP_644813.1:p.Cys271Ter