Canonical Allele Identifier: CA7989928

Gene: LAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28986429G>A , CM000678.2:g.28986429G>A	GRCh38
NC_000016.9:g.28997750G>A , CM000678.1:g.28997750G>A	GRCh37
NC_000016.8:g.28905251G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001014987.2:c.293G>A MANE Select	NP_001014987.1:p.Arg98Gln
ENST00000395456.7:c.293G>A MANE Select	ENSP00000378841.3:p.Arg98Gln
NM_001014987.1:c.293G>A	NP_001014987.1:p.Arg98Gln
NM_001014988.1:c.290G>A	NP_001014988.1:p.Arg97Gln
NM_001014988.2:c.290G>A	NP_001014988.1:p.Arg97Gln
NM_001014989.1:c.401G>A	NP_001014989.2:p.Arg134Gln
NM_001014989.2:c.401G>A	NP_001014989.2:p.Arg134Gln
NM_014387.3:c.293G>A	NP_055202.1:p.Arg98Gln
NM_014387.4:c.293G>A	NP_055202.1:p.Arg98Gln
ENST00000354453.7:n.616-1G>A
ENST00000360872.9:c.293G>A	ENSP00000354119.5:p.Arg98Gln
ENST00000395456.6:c.293G>A	ENSP00000378841.2:p.Arg98Gln
ENST00000395461.7:c.401G>A	ENSP00000378845.3:p.Arg134Gln
ENST00000454369.6:c.290G>A	ENSP00000398793.2:p.Arg97Gln
ENST00000562701.5:c.320G>A	ENSP00000454793.1:n.320G>A
ENST00000563964.5:n.560G>A
ENST00000564277.5:c.290G>A	ENSP00000457036.1:p.Arg97Gln
ENST00000566177.5:c.290G>A	ENSP00000456761.1:p.Arg97Gln
ENST00000568440.1:n.331G>A
ENST00000568899.5:n.177G>A
ENST00000570232.2:c.53G>A	ENSP00000455728.1:p.Arg18Gln
ENST00000697038.1:n.546G>A