Canonical Allele Identifier: CA338378815
Gene: MTOR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11109372T>G , CM000663.2:g.11109372T>G GRCh38
NC_000001.10:g.11169429T>G , CM000663.1:g.11169429T>G GRCh37
NC_000001.9:g.11092016T>G NCBI36
NG_033239.1:g.158180A>C , LRG_734:g.158180A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.*2823-2A>C ENSP00000515181.1:n.*2823-2A>C
ENST00000703131.1:n.3366-2A>C
ENST00000703139.1:c.2236-2A>C
ENST00000703140.1:c.7235-2A>C ENSP00000515197.1:n.7235-2A>C
ENST00000703141.1:c.*2965-2A>C ENSP00000515198.1:n.*2965-2A>C
ENST00000703142.1:c.*4278-2A>C ENSP00000515199.1:n.*4278-2A>C
ENST00000361445.9:c.7448-2A>C MANE Select ENSP00000354558.4:n.7448-2A>C
ENST00000361445.8:c.7448-2A>C ENSP00000354558.4:n.7448-2A>C
ENST00000376838.5:c.2063-2A>C ENSP00000366034.1:n.2063-2A>C
ENST00000455339.1:c.416-2A>C ENSP00000398745.1:n.416-2A>C
ENST00000473471.5:n.460-2A>C
ENST00000490931.1:n.731-2A>C
NM_004958.3:c.7448-2A>C , LRG_734t1:c.7448-2A>C NP_004949.1:n.7448-2A>C
XM_005263438.1:c.7448-2A>C XP_005263495.1:n.7448-2A>C
XM_005263438.2:c.7448-2A>C XP_005263495.1:n.7448-2A>C
XM_017000900.1:c.6767-2A>C XP_016856389.1:n.6767-2A>C
XM_017000901.1:c.6200-2A>C XP_016856390.1:n.6200-2A>C
XM_024446187.1:c.7448-2A>C XP_024301955.1:n.7448-2A>C
XR_001737087.1:n.7486-2A>C
NM_004958.4:c.7448-2A>C MANE Select NP_004949.1:n.7448-2A>C
NM_001386500.1:c.7448-2A>C NP_001373429.1:n.7448-2A>C
NM_001386501.1:c.6200-2A>C NP_001373430.1:n.6200-2A>C