Canonical Allele Identifier: CA338383476
Gene: MTOR HGNC NCBI

Linked Data

dbSNP Id: rs878855328
COSMIC: COSM4413485
MyVariant Identifiers: chr1:g.11177096C>A (hg19) chr1:g.11117039C>A (hg38)
CIViC: CA338383476
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11117039C>A , CM000663.2:g.11117039C>A GRCh38
NC_000001.10:g.11177096C>A , CM000663.1:g.11177096C>A GRCh37
NC_000001.9:g.11099683C>A NCBI36
NG_033239.1:g.150513G>T , LRG_734:g.150513G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000703118.1:c.*2356G>T ENSP00000515181.1:n.*2356G>T
ENST00000703131.1:n.2935-1571G>T
ENST00000703139.1:c.1769G>T
ENST00000703140.1:c.6768G>T ENSP00000515197.1:p.Met2256Ile
ENST00000703141.1:c.*2498G>T ENSP00000515198.1:n.*2498G>T
ENST00000703142.1:c.*3811G>T ENSP00000515199.1:n.*3811G>T
ENST00000361445.9:c.6981G>T MANE Select ENSP00000354558.4:p.Met2327Ile
ENST00000361445.8:c.6981G>T ENSP00000354558.4:p.Met2327Ile
ENST00000376838.5:c.1596G>T ENSP00000366034.1:p.Met532Ile
NM_004958.3:c.6981G>T , LRG_734t1:c.6981G>T NP_004949.1:p.Met2327Ile
XM_005263438.1:c.6981G>T XP_005263495.1:p.Met2327Ile
XR_244786.1:n.7055-1571G>T
XM_005263438.2:c.6981G>T XP_005263495.1:p.Met2327Ile
XM_017000900.1:c.6300G>T XP_016856389.1:p.Met2100Ile
XM_017000901.1:c.5733G>T XP_016856390.1:p.Met1911Ile
XM_024446187.1:c.6981G>T XP_024301955.1:p.Met2327Ile
XR_001737087.1:n.7055-1571G>T
NM_004958.4:c.6981G>T MANE Select NP_004949.1:p.Met2327Ile
NM_001386500.1:c.6981G>T NP_001373429.1:p.Met2327Ile
NM_001386501.1:c.5733G>T NP_001373430.1:p.Met1911Ile
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