Canonical Allele Identifier: CA415909452
Gene: MTOR HGNC NCBI
MTOR-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11145025G>A , CM000663.2:g.11145025G>A GRCh38
NC_000001.10:g.11205082G>A , CM000663.1:g.11205082G>A GRCh37
NC_000001.9:g.11127669G>A NCBI36
NG_033239.1:g.122527C>T , LRG_734:g.122527C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.*82C>T (MTOR) ENSP00000515181.1:n.*82C>T
ENST00000703131.1:n.627C>T (MTOR)
ENST00000703140.1:c.4494C>T (MTOR) ENSP00000515197.1:p.Asp1498=
ENST00000703141.1:c.4707C>T (MTOR) ENSP00000515198.1:p.Asp1569=
ENST00000703142.1:c.*1537C>T (MTOR) ENSP00000515199.1:n.*1537C>T
ENST00000361445.9:c.4707C>T (MTOR) MANE Select ENSP00000354558.4:p.Asp1569=
ENST00000361445.8:c.4707C>T (MTOR) ENSP00000354558.4:p.Asp1569=
ENST00000495435.1:n.1C>T (MTOR)
NM_004958.3:c.4707C>T , LRG_734t1:c.4707C>T (MTOR) NP_004949.1:p.Asp1569=
NR_046600.1:n.311-128G>A (MTOR-AS1)
XM_005263438.1:c.4707C>T (MTOR) XP_005263495.1:p.Asp1569=
XM_011541166.1:c.4707C>T (MTOR) XP_011539468.1:p.Asp1569=
XR_244786.1:n.4828C>T (MTOR)
XM_005263438.2:c.4707C>T (MTOR) XP_005263495.1:p.Asp1569=
XM_011541166.2:c.4707C>T (MTOR) XP_011539468.1:p.Asp1569=
XM_017000900.1:c.4026C>T (MTOR) XP_016856389.1:p.Asp1342=
XM_017000901.1:c.3459C>T (MTOR) XP_016856390.1:p.Asp1153=
XM_024446187.1:c.4707C>T (MTOR) XP_024301955.1:p.Asp1569=
XR_001737087.1:n.4828C>T (MTOR)
NM_004958.4:c.4707C>T (MTOR) MANE Select NP_004949.1:p.Asp1569=
NM_001386500.1:c.4707C>T (MTOR) NP_001373429.1:p.Asp1569=
NM_001386501.1:c.3459C>T (MTOR) NP_001373430.1:p.Asp1153=