Canonical Allele Identifier: CA338378535
Gene: MTOR HGNC NCBI

Linked Data

dbSNP Id: rs2100286589

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11109298T>C , CM000663.2:g.11109298T>C GRCh38
NC_000001.10:g.11169355T>C , CM000663.1:g.11169355T>C GRCh37
NC_000001.9:g.11091942T>C NCBI36
NG_033239.1:g.158254A>G , LRG_734:g.158254A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.*2895A>G ENSP00000515181.1:n.*2895A>G
ENST00000703131.1:n.3438A>G
ENST00000703139.1:c.2308A>G
ENST00000703140.1:c.7307A>G ENSP00000515197.1:p.Lys2436Arg
ENST00000703141.1:c.*3037A>G ENSP00000515198.1:n.*3037A>G
ENST00000703142.1:c.*4350A>G ENSP00000515199.1:n.*4350A>G
ENST00000361445.9:c.7520A>G MANE Select ENSP00000354558.4:p.Lys2507Arg
ENST00000361445.8:c.7520A>G ENSP00000354558.4:p.Lys2507Arg
ENST00000376838.5:c.2135A>G ENSP00000366034.1:p.Lys712Arg
ENST00000473471.5:n.532A>G
ENST00000490931.1:n.803A>G
NM_004958.3:c.7520A>G , LRG_734t1:c.7520A>G NP_004949.1:p.Lys2507Arg
XM_005263438.1:c.7520A>G XP_005263495.1:p.Lys2507Arg
XM_005263438.2:c.7520A>G XP_005263495.1:p.Lys2507Arg
XM_017000900.1:c.6839A>G XP_016856389.1:p.Lys2280Arg
XM_017000901.1:c.6272A>G XP_016856390.1:p.Lys2091Arg
XM_024446187.1:c.7520A>G XP_024301955.1:p.Lys2507Arg
XR_001737087.1:n.7558A>G
NM_004958.4:c.7520A>G MANE Select NP_004949.1:p.Lys2507Arg
NM_001386500.1:c.7520A>G NP_001373429.1:p.Lys2507Arg
NM_001386501.1:c.6272A>G NP_001373430.1:p.Lys2091Arg