Canonical Allele Identifier: CA1140490461
Gene: MTOR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11248017G= , CM000663.2:g.11248017G= GRCh38
NC_000001.10:g.11308074G= , CM000663.1:g.11308074G= GRCh37
NC_000001.9:g.11230661G= NCBI36
NG_033239.1:g.19535C= , LRG_734:g.19535C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.918C= ENSP00000515181.1:p.Phe306=
ENST00000703132.1:n.899C=
ENST00000703140.1:c.918C= ENSP00000515197.1:p.Phe306=
ENST00000703141.1:c.918C= ENSP00000515198.1:p.Phe306=
ENST00000703142.1:c.918C= ENSP00000515199.1:p.Phe306=
ENST00000703143.1:c.918C= ENSP00000515200.1:p.Phe306=
ENST00000361445.9:c.918C= MANE Select ENSP00000354558.4:p.Phe306=
ENST00000361445.8:c.918C= ENSP00000354558.4:p.Phe306=
NM_004958.3:c.918C= , LRG_734t1:c.918C= NP_004949.1:p.Phe306=
XM_005263438.1:c.918C= XP_005263495.1:p.Phe306=
XM_011541166.1:c.918C= XP_011539468.1:p.Phe306=
XR_244786.1:n.1039C=
XM_005263438.2:c.918C= XP_005263495.1:p.Phe306=
XM_011541166.2:c.918C= XP_011539468.1:p.Phe306=
XM_017000900.1:c.237C= XP_016856389.1:p.Phe79=
XM_017000901.1:c.-222C= XP_016856390.1:n.-222C=
XM_017000902.1:c.918C= XP_016856391.1:p.Phe306=
XM_024446187.1:c.918C= XP_024301955.1:p.Phe306=
XR_001737087.1:n.1039C=
NM_004958.4:c.918C= MANE Select NP_004949.1:p.Phe306=
NM_001386500.1:c.918C= NP_001373429.1:p.Phe306=
NM_001386501.1:c.-222C= NP_001373430.1:n.-222C=
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