Canonical Allele Identifier: CA1153594458
Gene: MTOR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11247747G= , CM000663.2:g.11247747G= GRCh38
NC_000001.10:g.11307804G= , CM000663.1:g.11307804G= GRCh37
NC_000001.9:g.11230391G= NCBI36
NG_033239.1:g.19805C= , LRG_734:g.19805C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.1117-14C= ENSP00000515181.1:n.1117-14C=
ENST00000703132.1:n.1097+72C=
ENST00000703140.1:c.1117-14C= ENSP00000515197.1:n.1117-14C=
ENST00000703141.1:c.1117-14C= ENSP00000515198.1:n.1117-14C=
ENST00000703142.1:c.1117-14C= ENSP00000515199.1:n.1117-14C=
ENST00000703143.1:c.1117-14C= ENSP00000515200.1:n.1117-14C=
ENST00000703144.1:n.87-14C=
ENST00000361445.9:c.1117-14C= MANE Select ENSP00000354558.4:n.1117-14C=
ENST00000361445.8:c.1117-14C= ENSP00000354558.4:n.1117-14C=
NM_004958.3:c.1117-14C= , LRG_734t1:c.1117-14C= NP_004949.1:n.1117-14C=
XM_005263438.1:c.1117-14C= XP_005263495.1:n.1117-14C=
XM_011541166.1:c.1117-14C= XP_011539468.1:n.1117-14C=
XR_244786.1:n.1238-14C=
XM_005263438.2:c.1117-14C= XP_005263495.1:n.1117-14C=
XM_011541166.2:c.1117-14C= XP_011539468.1:n.1117-14C=
XM_017000900.1:c.436-14C= XP_016856389.1:n.436-14C=
XM_017000901.1:c.-24+72C= XP_016856390.1:n.-24+72C=
XM_017000902.1:c.1117-14C= XP_016856391.1:n.1117-14C=
XM_024446187.1:c.1117-14C= XP_024301955.1:n.1117-14C=
XR_001737087.1:n.1238-14C=
NM_004958.4:c.1117-14C= MANE Select NP_004949.1:n.1117-14C=
NM_001386500.1:c.1117-14C= NP_001373429.1:n.1117-14C=
NM_001386501.1:c.-24+72C= NP_001373430.1:n.-24+72C=
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