Canonical Allele Identifier: CA7989955

Gene: LAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28986574G>A , CM000678.2:g.28986574G>A	GRCh38
NC_000016.9:g.28997895G>A , CM000678.1:g.28997895G>A	GRCh37
NC_000016.8:g.28905396G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697038.1:n.593+5G>A
ENST00000354453.7:n.667G>A
ENST00000395456.7:c.340+5G>A MANE Select	ENSP00000378841.3:n.340+5G>A
ENST00000360872.9:c.345G>A	ENSP00000354119.5:p.Ala115=
ENST00000395456.6:c.340+5G>A	ENSP00000378841.2:n.340+5G>A
ENST00000395461.7:c.448+5G>A	ENSP00000378845.3:n.448+5G>A
ENST00000454369.6:c.337+5G>A	ENSP00000398793.2:n.337+5G>A
ENST00000562701.5:c.372G>A	ENSP00000454793.1:n.372G>A
ENST00000563964.5:n.607+5G>A
ENST00000564277.5:c.337+5G>A	ENSP00000457036.1:n.337+5G>A
ENST00000566177.5:c.342G>A	ENSP00000456761.1:p.Ala114=
ENST00000568440.1:n.378+5G>A
ENST00000568899.5:n.224+5G>A
ENST00000570232.2:c.100+5G>A	ENSP00000455728.1:n.100+5G>A
NM_001014987.1:c.340+5G>A	NP_001014987.1:n.340+5G>A
NM_001014988.1:c.337+5G>A	NP_001014988.1:n.337+5G>A
NM_001014989.1:c.448+5G>A	NP_001014989.2:n.448+5G>A
NM_014387.3:c.345G>A	NP_055202.1:p.Ala115=
NM_001014987.2:c.340+5G>A MANE Select	NP_001014987.1:n.340+5G>A
NM_001014988.2:c.337+5G>A	NP_001014988.1:n.337+5G>A
NM_001014989.2:c.448+5G>A	NP_001014989.2:n.448+5G>A
NM_014387.4:c.345G>A	NP_055202.1:p.Ala115=