Canonical Allele Identifier: CA405308078

Gene: LGI4

Linked Data

• MyVariant Identifiers: chr19:g.35617753T>A (hg19) ; chr19:g.35126849T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35126849T>A , CM000681.2:g.35126849T>A	GRCh38
NC_000019.9:g.35617753T>A , CM000681.1:g.35617753T>A	GRCh37
NC_000019.8:g.40309593T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310123.8:c.793+4A>T MANE Select	ENSP00000312273.3:n.793+4A>T
ENST00000310123.7:c.793+4A>T	ENSP00000312273.3:n.793+4A>T
ENST00000392225.7:c.797A>T	ENSP00000376059.3:p.Glu266Val
ENST00000493050.5:n.852+4A>T
ENST00000587780.5:c.528+4A>T
ENST00000591840.5:n.420-1983A>T
ENST00000593248.5:n.928A>T
NM_139284.2:c.793+4A>T	NP_644813.1:n.793+4A>T
XM_011526594.1:c.793+4A>T	XP_011524896.1:n.793+4A>T
XM_011526595.1:c.277+4A>T	XP_011524897.1:n.277+4A>T
XM_011526595.2:c.277+4A>T	XP_011524897.1:n.277+4A>T
XM_017026428.1:c.277+4A>T	XP_016881917.1:n.277+4A>T
XM_017026429.1:c.277+4A>T	XP_016881918.1:n.277+4A>T
XM_017026430.2:c.277+4A>T	XP_016881919.1:n.277+4A>T
NM_139284.3:c.793+4A>T MANE Select	NP_644813.1:n.793+4A>T