Canonical Allele Identifier: CA405307260

Gene: LGI4

Linked Data

• gnomAD v4: 19-35126758-A-G
• MyVariant Identifiers: chr19:g.35617662A>G (hg19) ; chr19:g.35126758A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35126758A>G , CM000681.2:g.35126758A>G	GRCh38
NC_000019.9:g.35617662A>G , CM000681.1:g.35617662A>G	GRCh37
NC_000019.8:g.40309502A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310123.8:c.811T>C MANE Select	ENSP00000312273.3:p.Cys271Arg
ENST00000310123.7:c.811T>C	ENSP00000312273.3:p.Cys271Arg
ENST00000392225.7:c.888T>C	ENSP00000376059.3:p.Pro296=
ENST00000493050.5:n.870T>C
ENST00000587780.5:c.546T>C
ENST00000591840.5:n.420-1892T>C
ENST00000593248.5:n.1019T>C
NM_139284.2:c.811T>C	NP_644813.1:p.Cys271Arg
XM_011526594.1:c.811T>C	XP_011524896.1:p.Cys271Arg
XM_011526595.1:c.295T>C	XP_011524897.1:p.Cys99Arg
XM_011526595.2:c.295T>C	XP_011524897.1:p.Cys99Arg
XM_017026428.1:c.295T>C	XP_016881917.1:p.Cys99Arg
XM_017026429.1:c.295T>C	XP_016881918.1:p.Cys99Arg
XM_017026430.2:c.295T>C	XP_016881919.1:p.Cys99Arg
NM_139284.3:c.811T>C MANE Select	NP_644813.1:p.Cys271Arg