Canonical Allele Identifier: CA405304273
Community Standard Title: NM_139284.3(LGI4):c.1153C>T (p.Gln385Ter)
Gene: LGI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35126416G>A , CM000681.2:g.35126416G>A GRCh38
NC_000019.9:g.35617320G>A , CM000681.1:g.35617320G>A GRCh37
NC_000019.8:g.40309160G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_139284.3:c.1153C>T MANE Select NP_644813.1:p.Gln385Ter
ENST00000310123.8:c.1153C>T MANE Select ENSP00000312273.3:p.Gln385Ter
NM_139284.2:c.1153C>T NP_644813.1:p.Gln385Ter
ENST00000310123.7:c.1153C>T ENSP00000312273.3:p.Gln385Ter
ENST00000392225.7:c.1230C>T ENSP00000376059.3:p.Pro410=
ENST00000493050.5:n.1212C>T
ENST00000587780.5:c.888C>T
ENST00000591840.5:n.420-1550C>T
XM_011526594.1:c.1153C>T XP_011524896.1:p.Gln385Ter
XM_011526595.1:c.637C>T XP_011524897.1:p.Gln213Ter
XM_011526595.2:c.637C>T XP_011524897.1:p.Gln213Ter
XM_017026428.1:c.637C>T XP_016881917.1:p.Gln213Ter
XM_017026429.1:c.637C>T XP_016881918.1:p.Gln213Ter
XM_017026430.2:c.637C>T XP_016881919.1:p.Gln213Ter