Canonical Allele Identifier: CA7989932

Gene: LAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28986446_28986448dup , CM000678.2:g.28986446_28986448dup	GRCh38
NC_000016.9:g.28997767_28997769dup , CM000678.1:g.28997767_28997769dup	GRCh37
NC_000016.8:g.28905268_28905270dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001014987.1:c.310_310+2dup
NM_001014987.2:c.310_310+2dup
NM_001014988.1:c.307_307+2dup
NM_001014988.2:c.307_307+2dup
NM_001014989.1:c.418_418+2dup
NM_001014989.2:c.418_418+2dup
NM_014387.3:c.310_310+2dup
NM_014387.4:c.310_310+2dup
ENST00000354453.7:n.632_632+2dup
ENST00000360872.9:c.310_310+2dup
ENST00000395456.6:c.310_310+2dup
ENST00000395456.7:c.310_310+2dup
ENST00000395461.7:c.418_418+2dup
ENST00000454369.6:c.307_307+2dup
ENST00000562701.5:c.337_337+2dup
ENST00000563964.5:n.577_577+2dup
ENST00000564277.5:c.307_307+2dup
ENST00000566177.5:c.307_307+2dup
ENST00000568440.1:n.348_348+2dup
ENST00000568899.5:n.194_194+2dup
ENST00000570232.2:c.70_70+2dup
ENST00000697038.1:n.563_563+2dup