Canonical Allele Identifier: CA589171

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11127738T>C , CM000663.2:g.11127738T>C	GRCh38
NC_000001.10:g.11187795T>C , CM000663.1:g.11187795T>C	GRCh37
NC_000001.9:g.11110382T>C	NCBI36
NG_033239.1:g.139814A>G , LRG_734:g.139814A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*1477A>G	ENSP00000515181.1:n.*1477A>G
ENST00000703131.1:n.2103A>G
ENST00000703139.1:c.739A>G
ENST00000703140.1:c.5889A>G	ENSP00000515197.1:p.Ala1963=
ENST00000703141.1:c.*1619A>G	ENSP00000515198.1:n.*1619A>G
ENST00000703142.1:c.*2932A>G	ENSP00000515199.1:n.*2932A>G
ENST00000361445.9:c.6102A>G MANE Select	ENSP00000354558.4:p.Ala2034=
ENST00000361445.8:c.6102A>G	ENSP00000354558.4:p.Ala2034=
ENST00000376838.5:c.717A>G	ENSP00000366034.1:p.Ala239=
NM_004958.3:c.6102A>G , LRG_734t1:c.6102A>G	NP_004949.1:p.Ala2034=
XM_005263438.1:c.6102A>G	XP_005263495.1:p.Ala2034=
XR_244786.1:n.6223A>G
XM_005263438.2:c.6102A>G	XP_005263495.1:p.Ala2034=
XM_017000900.1:c.5421A>G	XP_016856389.1:p.Ala1807=
XM_017000901.1:c.4854A>G	XP_016856390.1:p.Ala1618=
XM_024446187.1:c.6102A>G	XP_024301955.1:p.Ala2034=
XR_001737087.1:n.6223A>G
NM_004958.4:c.6102A>G MANE Select	NP_004949.1:p.Ala2034=
NM_001386500.1:c.6102A>G	NP_001373429.1:p.Ala2034=
NM_001386501.1:c.4854A>G	NP_001373430.1:p.Ala1618=