Canonical Allele Identifier: CA279252807

Gene: LAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28986530C>G , CM000678.2:g.28986530C>G	GRCh38
NC_000016.9:g.28997851C>G , CM000678.1:g.28997851C>G	GRCh37
NC_000016.8:g.28905352C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001014987.2:c.311-10C>G MANE Select	NP_001014987.1:n.311-10C>G
ENST00000395456.7:c.311-10C>G MANE Select	ENSP00000378841.3:n.311-10C>G
NM_001014987.1:c.311-10C>G	NP_001014987.1:n.311-10C>G
NM_001014988.1:c.308-10C>G	NP_001014988.1:n.308-10C>G
NM_001014988.2:c.308-10C>G	NP_001014988.1:n.308-10C>G
NM_001014989.1:c.419-10C>G	NP_001014989.2:n.419-10C>G
NM_001014989.2:c.419-10C>G	NP_001014989.2:n.419-10C>G
NM_014387.3:c.311-10C>G	NP_055202.1:n.311-10C>G
NM_014387.4:c.311-10C>G	NP_055202.1:n.311-10C>G
ENST00000354453.7:n.633-10C>G
ENST00000360872.9:c.311-10C>G	ENSP00000354119.5:n.311-10C>G
ENST00000395456.6:c.311-10C>G	ENSP00000378841.2:n.311-10C>G
ENST00000395461.7:c.419-10C>G	ENSP00000378845.3:n.419-10C>G
ENST00000454369.6:c.308-10C>G	ENSP00000398793.2:n.308-10C>G
ENST00000562701.5:c.338-10C>G	ENSP00000454793.1:n.338-10C>G
ENST00000563964.5:n.578-10C>G
ENST00000564277.5:c.308-10C>G	ENSP00000457036.1:n.308-10C>G
ENST00000566177.5:c.308-10C>G	ENSP00000456761.1:n.308-10C>G
ENST00000568440.1:n.349-10C>G
ENST00000568899.5:n.195-10C>G
ENST00000570232.2:c.71-10C>G	ENSP00000455728.1:n.71-10C>G
ENST00000697038.1:n.564-10C>G