Canonical Allele Identifier: CA405315145
Community Standard Title: NM_139284.3(LGI4):c.200T>G (p.Leu67Arg)
Gene: LGI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35134075A>C , CM000681.2:g.35134075A>C GRCh38
NC_000019.9:g.35624979A>C , CM000681.1:g.35624979A>C GRCh37
NC_000019.8:g.40316819A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_139284.3:c.200T>G MANE Select NP_644813.1:p.Leu67Arg
ENST00000310123.8:c.200T>G MANE Select ENSP00000312273.3:p.Leu67Arg
NM_139284.2:c.200T>G NP_644813.1:p.Leu67Arg
ENST00000310123.7:c.200T>G ENSP00000312273.3:p.Leu67Arg
ENST00000392225.7:c.200T>G ENSP00000376059.3:p.Leu67Arg
ENST00000473160.6:n.158T>G
ENST00000493050.5:n.259T>G
ENST00000591633.2:c.200T>G ENSP00000467784.1:p.Leu67Arg
ENST00000591840.5:n.163T>G
ENST00000592346.1:n.148T>G
XM_011526594.1:c.200T>G XP_011524896.1:p.Leu67Arg
XM_011526595.1:c.-444T>G XP_011524897.1:n.-444T>G
XM_011526595.2:c.-444T>G XP_011524897.1:n.-444T>G
XM_017026428.1:c.-317T>G XP_016881917.1:n.-317T>G
XM_017026429.1:c.-389T>G XP_016881918.1:n.-389T>G