Canonical Allele Identifier: CA405308149

Gene: LGI4

Linked Data

• MyVariant Identifiers: chr19:g.35617762A>C (hg19) ; chr19:g.35126858A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35126858A>C , CM000681.2:g.35126858A>C	GRCh38
NC_000019.9:g.35617762A>C , CM000681.1:g.35617762A>C	GRCh37
NC_000019.8:g.40309602A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310123.8:c.788T>G MANE Select	ENSP00000312273.3:p.Leu263Arg
ENST00000310123.7:c.788T>G	ENSP00000312273.3:p.Leu263Arg
ENST00000392225.7:c.788T>G	ENSP00000376059.3:p.Leu263Arg
ENST00000493050.5:n.847T>G
ENST00000587780.5:c.523T>G
ENST00000591840.5:n.420-1992T>G
ENST00000593248.5:n.919T>G
NM_139284.2:c.788T>G	NP_644813.1:p.Leu263Arg
XM_011526594.1:c.788T>G	XP_011524896.1:p.Leu263Arg
XM_011526595.1:c.272T>G	XP_011524897.1:p.Leu91Arg
XM_011526595.2:c.272T>G	XP_011524897.1:p.Leu91Arg
XM_017026428.1:c.272T>G	XP_016881917.1:p.Leu91Arg
XM_017026429.1:c.272T>G	XP_016881918.1:p.Leu91Arg
XM_017026430.2:c.272T>G	XP_016881919.1:p.Leu91Arg
NM_139284.3:c.788T>G MANE Select	NP_644813.1:p.Leu263Arg