Canonical Allele Identifier: CA2841556712
Gene: MTOR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11247830dup , CM000663.2:g.11247830dup GRCh38
NC_000001.10:g.11307887dup , CM000663.1:g.11307887dup GRCh37
NC_000001.9:g.11230474dup NCBI36
NG_033239.1:g.19724dup , LRG_734:g.19724dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.1107dup ENSP00000515181.1:p.Phe370IlefsTer2
ENST00000703132.1:n.1088dup
ENST00000703140.1:c.1107dup ENSP00000515197.1:p.Phe370IlefsTer2
ENST00000703141.1:c.1107dup ENSP00000515198.1:p.Phe370IlefsTer2
ENST00000703142.1:c.1107dup ENSP00000515199.1:p.Phe370IlefsTer2
ENST00000703143.1:c.1107dup ENSP00000515200.1:p.Phe370IlefsTer2
ENST00000703144.1:n.77dup
ENST00000361445.9:c.1107dup MANE Select ENSP00000354558.4:p.Phe370IlefsTer2
ENST00000361445.8:c.1107dup ENSP00000354558.4:p.Phe370IlefsTer2
NM_004958.3:c.1107dup , LRG_734t1:c.1107dup NP_004949.1:p.Phe370IlefsTer2
XM_005263438.1:c.1107dup XP_005263495.1:p.Phe370IlefsTer2
XM_011541166.1:c.1107dup XP_011539468.1:p.Phe370IlefsTer2
XR_244786.1:n.1228dup
XM_005263438.2:c.1107dup XP_005263495.1:p.Phe370IlefsTer2
XM_011541166.2:c.1107dup XP_011539468.1:p.Phe370IlefsTer2
XM_017000900.1:c.426dup XP_016856389.1:p.Phe143IlefsTer2
XM_017000901.1:c.-33dup XP_016856390.1:n.-33dup
XM_017000902.1:c.1107dup XP_016856391.1:p.Phe370IlefsTer2
XM_024446187.1:c.1107dup XP_024301955.1:p.Phe370IlefsTer2
XR_001737087.1:n.1228dup
NM_004958.4:c.1107dup MANE Select NP_004949.1:p.Phe370IlefsTer2
NM_001386500.1:c.1107dup NP_001373429.1:p.Phe370IlefsTer2
NM_001386501.1:c.-33dup NP_001373430.1:n.-33dup