Canonical Allele Identifier: CA405308116

Gene: LGI4

Linked Data

• MyVariant Identifiers: chr19:g.35617757C>G (hg19) ; chr19:g.35126853C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35126853C>G , CM000681.2:g.35126853C>G	GRCh38
NC_000019.9:g.35617757C>G , CM000681.1:g.35617757C>G	GRCh37
NC_000019.8:g.40309597C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310123.8:c.793G>C MANE Select	ENSP00000312273.3:p.Ala265Pro
ENST00000310123.7:c.793G>C	ENSP00000312273.3:p.Ala265Pro
ENST00000392225.7:c.793G>C	ENSP00000376059.3:p.Gly265Arg
ENST00000493050.5:n.852G>C
ENST00000587780.5:c.528G>C
ENST00000591840.5:n.420-1987G>C
ENST00000593248.5:n.924G>C
NM_139284.2:c.793G>C	NP_644813.1:p.Ala265Pro
XM_011526594.1:c.793G>C	XP_011524896.1:p.Ala265Pro
XM_011526595.1:c.277G>C	XP_011524897.1:p.Ala93Pro
XM_011526595.2:c.277G>C	XP_011524897.1:p.Ala93Pro
XM_017026428.1:c.277G>C	XP_016881917.1:p.Ala93Pro
XM_017026429.1:c.277G>C	XP_016881918.1:p.Ala93Pro
XM_017026430.2:c.277G>C	XP_016881919.1:p.Ala93Pro
NM_139284.3:c.793G>C MANE Select	NP_644813.1:p.Ala265Pro