Canonical Allele Identifier: CA507294143

Gene: LGI4

Linked Data

• MyVariant Identifiers: chr19:g.35617839C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35126935C>A , CM000681.2:g.35126935C>A	GRCh38
NC_000019.9:g.35617839C>A , CM000681.1:g.35617839C>A	GRCh37
NC_000019.8:g.40309679C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310123.8:c.711G>T MANE Select	ENSP00000312273.3:p.Leu237=
ENST00000310123.7:c.711G>T	ENSP00000312273.3:p.Leu237=
ENST00000392225.7:c.711G>T	ENSP00000376059.3:p.Leu237=
ENST00000493050.5:n.770G>T
ENST00000587780.5:c.446G>T
ENST00000591840.5:n.420-2069G>T
ENST00000593248.5:n.842G>T
NM_139284.2:c.711G>T	NP_644813.1:p.Leu237=
XM_011526594.1:c.711G>T	XP_011524896.1:p.Leu237=
XM_011526595.1:c.195G>T	XP_011524897.1:p.Leu65=
XM_011526595.2:c.195G>T	XP_011524897.1:p.Leu65=
XM_017026428.1:c.195G>T	XP_016881917.1:p.Leu65=
XM_017026429.1:c.195G>T	XP_016881918.1:p.Leu65=
XM_017026430.2:c.195G>T	XP_016881919.1:p.Leu65=
NM_139284.3:c.711G>T MANE Select	NP_644813.1:p.Leu237=