Canonical Allele Identifier: CA9373472
Community Standard Title: NM_139284.3(LGI4):c.61A>T (p.Arg21Ter)
Gene: LGI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35134620T>A , CM000681.2:g.35134620T>A GRCh38
NC_000019.9:g.35625524T>A , CM000681.1:g.35625524T>A GRCh37
NC_000019.8:g.40317364T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_139284.3:c.61A>T MANE Select NP_644813.1:p.Arg21Ter
ENST00000310123.8:c.61A>T MANE Select ENSP00000312273.3:p.Arg21Ter
NM_139284.2:c.61A>T NP_644813.1:p.Arg21Ter
ENST00000310123.7:c.61A>T ENSP00000312273.3:p.Arg21Ter
ENST00000392225.7:c.61A>T ENSP00000376059.3:p.Arg21Ter
ENST00000473160.6:n.19A>T
ENST00000493050.5:n.183-63A>T
ENST00000591633.2:c.61A>T ENSP00000467784.1:p.Arg21Ter
ENST00000591840.5:n.24A>T
ENST00000592346.1:n.9A>T
XM_011526594.1:c.61A>T XP_011524896.1:p.Arg21Ter
XM_011526595.1:c.-583A>T XP_011524897.1:n.-583A>T
XM_011526595.2:c.-583A>T XP_011524897.1:n.-583A>T