Canonical Allele Identifier: CA7990041

Gene: LAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28989487C>T , CM000678.2:g.28989487C>T	GRCh38
NC_000016.9:g.29000808C>T , CM000678.1:g.29000808C>T	GRCh37
NC_000016.8:g.28908309C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001014987.2:c.494-40C>T MANE Select	NP_001014987.1:n.494-40C>T
ENST00000395456.7:c.494-40C>T MANE Select	ENSP00000378841.3:n.494-40C>T
NM_001014987.1:c.494-40C>T	NP_001014987.1:n.494-40C>T
NM_001014988.1:c.491-40C>T	NP_001014988.1:n.491-40C>T
NM_001014988.2:c.491-40C>T	NP_001014988.1:n.491-40C>T
NM_001014989.1:c.602-40C>T	NP_001014989.2:n.602-40C>T
NM_001014989.2:c.602-40C>T	NP_001014989.2:n.602-40C>T
NM_014387.3:c.581-40C>T	NP_055202.1:n.581-40C>T
NM_014387.4:c.581-40C>T	NP_055202.1:n.581-40C>T
ENST00000354453.7:n.903-40C>T
ENST00000360872.9:c.581-40C>T	ENSP00000354119.5:n.581-40C>T
ENST00000395456.6:c.494-40C>T	ENSP00000378841.2:n.494-40C>T
ENST00000395461.7:c.602-40C>T	ENSP00000378845.3:n.602-40C>T
ENST00000454369.6:c.491-40C>T	ENSP00000398793.2:n.491-40C>T
ENST00000562701.5:c.608-40C>T	ENSP00000454793.1:n.608-40C>T
ENST00000564277.5:c.491-40C>T	ENSP00000457036.1:n.491-40C>T
ENST00000564447.5:n.1922C>T
ENST00000566177.5:c.578-40C>T	ENSP00000456761.1:n.578-40C>T
ENST00000568899.5:n.378-40C>T
ENST00000570232.2:c.254-40C>T	ENSP00000455728.1:n.254-40C>T
ENST00000697038.1:n.747-40C>T