Canonical Allele Identifier: CA338366691
Gene: MTOR HGNC NCBI
MTOR-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11145002G>A , CM000663.2:g.11145002G>A GRCh38
NC_000001.10:g.11205059G>A , CM000663.1:g.11205059G>A GRCh37
NC_000001.9:g.11127646G>A NCBI36
NG_033239.1:g.122550C>T , LRG_734:g.122550C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.*105C>T (MTOR) ENSP00000515181.1:n.*105C>T
ENST00000703131.1:n.650C>T (MTOR)
ENST00000703140.1:c.4517C>T (MTOR) ENSP00000515197.1:p.Ala1506Val
ENST00000703141.1:c.4730C>T (MTOR) ENSP00000515198.1:p.Ala1577Val
ENST00000703142.1:c.*1560C>T (MTOR) ENSP00000515199.1:n.*1560C>T
ENST00000361445.9:c.4730C>T (MTOR) MANE Select ENSP00000354558.4:p.Ala1577Val
ENST00000361445.8:c.4730C>T (MTOR) ENSP00000354558.4:p.Ala1577Val
ENST00000495435.1:n.24C>T (MTOR)
NM_004958.3:c.4730C>T , LRG_734t1:c.4730C>T (MTOR) NP_004949.1:p.Ala1577Val
NR_046600.1:n.310+116G>A (MTOR-AS1)
XM_005263438.1:c.4730C>T (MTOR) XP_005263495.1:p.Ala1577Val
XM_011541166.1:c.4730C>T (MTOR) XP_011539468.1:p.Ala1577Val
XR_244786.1:n.4851C>T (MTOR)
XM_005263438.2:c.4730C>T (MTOR) XP_005263495.1:p.Ala1577Val
XM_011541166.2:c.4730C>T (MTOR) XP_011539468.1:p.Ala1577Val
XM_017000900.1:c.4049C>T (MTOR) XP_016856389.1:p.Ala1350Val
XM_017000901.1:c.3482C>T (MTOR) XP_016856390.1:p.Ala1161Val
XM_024446187.1:c.4730C>T (MTOR) XP_024301955.1:p.Ala1577Val
XR_001737087.1:n.4851C>T (MTOR)
NM_004958.4:c.4730C>T (MTOR) MANE Select NP_004949.1:p.Ala1577Val
NM_001386500.1:c.4730C>T (MTOR) NP_001373429.1:p.Ala1577Val
NM_001386501.1:c.3482C>T (MTOR) NP_001373430.1:p.Ala1161Val