Canonical Allele Identifier: CA405308885

Gene: LGI4

Linked Data

• MyVariant Identifiers: chr19:g.35617850G>T (hg19) ; chr19:g.35126946G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35126946G>T , CM000681.2:g.35126946G>T	GRCh38
NC_000019.9:g.35617850G>T , CM000681.1:g.35617850G>T	GRCh37
NC_000019.8:g.40309690G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310123.8:c.700C>A MANE Select	ENSP00000312273.3:p.His234Asn
ENST00000310123.7:c.700C>A	ENSP00000312273.3:p.His234Asn
ENST00000392225.7:c.700C>A	ENSP00000376059.3:p.His234Asn
ENST00000493050.5:n.759C>A
ENST00000587780.5:c.435C>A
ENST00000591840.5:n.420-2080C>A
ENST00000593248.5:n.831C>A
NM_139284.2:c.700C>A	NP_644813.1:p.His234Asn
XM_011526594.1:c.700C>A	XP_011524896.1:p.His234Asn
XM_011526595.1:c.184C>A	XP_011524897.1:p.His62Asn
XM_011526595.2:c.184C>A	XP_011524897.1:p.His62Asn
XM_017026428.1:c.184C>A	XP_016881917.1:p.His62Asn
XM_017026429.1:c.184C>A	XP_016881918.1:p.His62Asn
XM_017026430.2:c.184C>A	XP_016881919.1:p.His62Asn
NM_139284.3:c.700C>A MANE Select	NP_644813.1:p.His234Asn