Canonical Allele Identifier: CA415916503
Gene: MTOR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.11169348A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11109291A>T , CM000663.2:g.11109291A>T GRCh38
NC_000001.10:g.11169348A>T , CM000663.1:g.11169348A>T GRCh37
NC_000001.9:g.11091935A>T NCBI36
NG_033239.1:g.158261T>A , LRG_734:g.158261T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.*2902T>A ENSP00000515181.1:n.*2902T>A
ENST00000703131.1:n.3445T>A
ENST00000703139.1:c.2315T>A
ENST00000703140.1:c.7314T>A ENSP00000515197.1:p.Thr2438=
ENST00000703141.1:c.*3044T>A ENSP00000515198.1:n.*3044T>A
ENST00000703142.1:c.*4357T>A ENSP00000515199.1:n.*4357T>A
ENST00000361445.9:c.7527T>A MANE Select ENSP00000354558.4:p.Thr2509=
ENST00000361445.8:c.7527T>A ENSP00000354558.4:p.Thr2509=
ENST00000376838.5:c.2142T>A ENSP00000366034.1:p.Thr714=
ENST00000473471.5:n.539T>A
ENST00000490931.1:n.810T>A
NM_004958.3:c.7527T>A , LRG_734t1:c.7527T>A NP_004949.1:p.Thr2509=
XM_005263438.1:c.7527T>A XP_005263495.1:p.Thr2509=
XM_005263438.2:c.7527T>A XP_005263495.1:p.Thr2509=
XM_017000900.1:c.6846T>A XP_016856389.1:p.Thr2282=
XM_017000901.1:c.6279T>A XP_016856390.1:p.Thr2093=
XM_024446187.1:c.7527T>A XP_024301955.1:p.Thr2509=
XR_001737087.1:n.7565T>A
NM_004958.4:c.7527T>A MANE Select NP_004949.1:p.Thr2509=
NM_001386500.1:c.7527T>A NP_001373429.1:p.Thr2509=
NM_001386501.1:c.6279T>A NP_001373430.1:p.Thr2093=