Canonical Allele Identifier: CA7989975

Gene: LAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28986675C>T , CM000678.2:g.28986675C>T	GRCh38
NC_000016.9:g.28997996C>T , CM000678.1:g.28997996C>T	GRCh37
NC_000016.8:g.28905497C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697038.1:n.612C>T
ENST00000354453.7:n.768C>T
ENST00000395456.7:c.359C>T MANE Select	ENSP00000378841.3:p.Ala120Val
ENST00000360872.9:c.446C>T	ENSP00000354119.5:p.Ala149Val
ENST00000395456.6:c.359C>T	ENSP00000378841.2:p.Ala120Val
ENST00000395461.7:c.467C>T	ENSP00000378845.3:p.Ala156Val
ENST00000454369.6:c.356C>T	ENSP00000398793.2:p.Ala119Val
ENST00000562701.5:c.473C>T	ENSP00000454793.1:n.473C>T
ENST00000563964.5:n.626C>T
ENST00000564277.5:c.356C>T	ENSP00000457036.1:p.Ala119Val
ENST00000566177.5:c.443C>T	ENSP00000456761.1:p.Ala148Val
ENST00000568440.1:n.397C>T
ENST00000568899.5:n.243C>T
ENST00000570232.2:c.119C>T	ENSP00000455728.1:p.Ala40Val
NM_001014987.1:c.359C>T	NP_001014987.1:p.Ala120Val
NM_001014988.1:c.356C>T	NP_001014988.1:p.Ala119Val
NM_001014989.1:c.467C>T	NP_001014989.2:p.Ala156Val
NM_014387.3:c.446C>T	NP_055202.1:p.Ala149Val
NM_001014987.2:c.359C>T MANE Select	NP_001014987.1:p.Ala120Val
NM_001014988.2:c.356C>T	NP_001014988.1:p.Ala119Val
NM_001014989.2:c.467C>T	NP_001014989.2:p.Ala156Val
NM_014387.4:c.446C>T	NP_055202.1:p.Ala149Val