Canonical Allele Identifier: CA338399433
Gene: MTOR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.11307895A>G (hg19) chr1:g.11247838A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11247838A>G , CM000663.2:g.11247838A>G GRCh38
NC_000001.10:g.11307895A>G , CM000663.1:g.11307895A>G GRCh37
NC_000001.9:g.11230482A>G NCBI36
NG_033239.1:g.19714T>C , LRG_734:g.19714T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.1097T>C ENSP00000515181.1:p.Met366Thr
ENST00000703132.1:n.1078T>C
ENST00000703140.1:c.1097T>C ENSP00000515197.1:p.Met366Thr
ENST00000703141.1:c.1097T>C ENSP00000515198.1:p.Met366Thr
ENST00000703142.1:c.1097T>C ENSP00000515199.1:p.Met366Thr
ENST00000703143.1:c.1097T>C ENSP00000515200.1:p.Met366Thr
ENST00000703144.1:n.67T>C
ENST00000361445.9:c.1097T>C MANE Select ENSP00000354558.4:p.Met366Thr
ENST00000361445.8:c.1097T>C ENSP00000354558.4:p.Met366Thr
NM_004958.3:c.1097T>C , LRG_734t1:c.1097T>C NP_004949.1:p.Met366Thr
XM_005263438.1:c.1097T>C XP_005263495.1:p.Met366Thr
XM_011541166.1:c.1097T>C XP_011539468.1:p.Met366Thr
XR_244786.1:n.1218T>C
XM_005263438.2:c.1097T>C XP_005263495.1:p.Met366Thr
XM_011541166.2:c.1097T>C XP_011539468.1:p.Met366Thr
XM_017000900.1:c.416T>C XP_016856389.1:p.Met139Thr
XM_017000901.1:c.-43T>C XP_016856390.1:n.-43T>C
XM_017000902.1:c.1097T>C XP_016856391.1:p.Met366Thr
XM_024446187.1:c.1097T>C XP_024301955.1:p.Met366Thr
XR_001737087.1:n.1218T>C
NM_004958.4:c.1097T>C MANE Select NP_004949.1:p.Met366Thr
NM_001386500.1:c.1097T>C NP_001373429.1:p.Met366Thr
NM_001386501.1:c.-43T>C NP_001373430.1:n.-43T>C
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