Canonical Allele Identifier: CA645615871

Gene: LGI4

Linked Data

• COSMIC: COSM6440134

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35126854_35126855delinsAA , CM000681.2:g.35126854_35126855delinsAA	GRCh38
NC_000019.9:g.35617758_35617759delinsAA , CM000681.1:g.35617758_35617759delinsAA	GRCh37
NC_000019.8:g.40309598_40309599delinsAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310123.8:c.791_792delinsTT MANE Select	ENSP00000312273.3:p.Pro264Leu
ENST00000310123.7:c.791_792delinsTT	ENSP00000312273.3:p.Pro264Leu
ENST00000392225.7:c.791_792delinsTT	ENSP00000376059.3:p.Pro264Leu
ENST00000493050.5:n.850_851delinsTT
ENST00000587780.5:c.526_527delinsTT
ENST00000591840.5:n.420-1989_420-1988delinsTT
ENST00000593248.5:n.922_923delinsTT
NM_139284.2:c.791_792delinsTT	NP_644813.1:p.Pro264Leu
XM_011526594.1:c.791_792delinsTT	XP_011524896.1:p.Pro264Leu
XM_011526595.1:c.275_276delinsTT	XP_011524897.1:p.Pro92Leu
XM_011526595.2:c.275_276delinsTT	XP_011524897.1:p.Pro92Leu
XM_017026428.1:c.275_276delinsTT	XP_016881917.1:p.Pro92Leu
XM_017026429.1:c.275_276delinsTT	XP_016881918.1:p.Pro92Leu
XM_017026430.2:c.275_276delinsTT	XP_016881919.1:p.Pro92Leu
NM_139284.3:c.791_792delinsTT MANE Select	NP_644813.1:p.Pro264Leu