Canonical Allele Identifier: CA338391533
Gene: MTOR HGNC NCBI

Linked Data

dbSNP Id: rs1642872553
COSMIC: COSM4439845
MyVariant Identifiers: chr1:g.11187094G>T (hg19) chr1:g.11127037G>T (hg38)
CIViC: CA338391533
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11127037G>T , CM000663.2:g.11127037G>T GRCh38
NC_000001.10:g.11187094G>T , CM000663.1:g.11187094G>T GRCh37
NC_000001.9:g.11109681G>T NCBI36
NG_033239.1:g.140515C>A , LRG_734:g.140515C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703118.1:c.*1699C>A ENSP00000515181.1:n.*1699C>A
ENST00000703131.1:n.2325C>A
ENST00000703139.1:c.961C>A
ENST00000703140.1:c.6111C>A ENSP00000515197.1:p.Phe2037Leu
ENST00000703141.1:c.*1841C>A ENSP00000515198.1:n.*1841C>A
ENST00000703142.1:c.*3154C>A ENSP00000515199.1:n.*3154C>A
ENST00000361445.9:c.6324C>A MANE Select ENSP00000354558.4:p.Phe2108Leu
ENST00000361445.8:c.6324C>A ENSP00000354558.4:p.Phe2108Leu
ENST00000376838.5:c.939C>A ENSP00000366034.1:p.Phe313Leu
NM_004958.3:c.6324C>A , LRG_734t1:c.6324C>A NP_004949.1:p.Phe2108Leu
XM_005263438.1:c.6324C>A XP_005263495.1:p.Phe2108Leu
XR_244786.1:n.6445C>A
XM_005263438.2:c.6324C>A XP_005263495.1:p.Phe2108Leu
XM_017000900.1:c.5643C>A XP_016856389.1:p.Phe1881Leu
XM_017000901.1:c.5076C>A XP_016856390.1:p.Phe1692Leu
XM_024446187.1:c.6324C>A XP_024301955.1:p.Phe2108Leu
XR_001737087.1:n.6445C>A
NM_004958.4:c.6324C>A MANE Select NP_004949.1:p.Phe2108Leu
NM_001386500.1:c.6324C>A NP_001373429.1:p.Phe2108Leu
NM_001386501.1:c.5076C>A NP_001373430.1:p.Phe1692Leu
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