Canonical Allele Identifier: CA405314801

Gene: LGI4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35133695G>T , CM000681.2:g.35133695G>T	GRCh38
NC_000019.9:g.35624599G>T , CM000681.1:g.35624599G>T	GRCh37
NC_000019.8:g.40316439G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_139284.3:c.312C>A MANE Select	NP_644813.1:p.Tyr104Ter
ENST00000310123.8:c.312C>A MANE Select	ENSP00000312273.3:p.Tyr104Ter
NM_139284.2:c.312C>A	NP_644813.1:p.Tyr104Ter
ENST00000310123.7:c.312C>A	ENSP00000312273.3:p.Tyr104Ter
ENST00000392225.7:c.312C>A	ENSP00000376059.3:p.Tyr104Ter
ENST00000473160.6:n.538C>A
ENST00000493050.5:n.371C>A
ENST00000587780.5:c.47C>A
ENST00000591633.2:c.312C>A	ENSP00000467784.1:p.Tyr104Ter
ENST00000591840.5:n.275C>A
ENST00000592346.1:n.260C>A
ENST00000593248.5:n.318C>A
XM_011526594.1:c.312C>A	XP_011524896.1:p.Tyr104Ter
XM_011526595.1:c.-332C>A	XP_011524897.1:n.-332C>A
XM_011526595.2:c.-332C>A	XP_011524897.1:n.-332C>A
XM_017026428.1:c.-205C>A	XP_016881917.1:n.-205C>A
XM_017026429.1:c.-277C>A	XP_016881918.1:n.-277C>A