Canonical Allele Identifier: CA590807
Gene: MTOR HGNC NCBI

Linked Data

dbSNP Id: rs748136346

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11247791_11247792del , CM000663.2:g.11247791_11247792del GRCh38
NC_000001.10:g.11307848_11307849del , CM000663.1:g.11307848_11307849del GRCh37
NC_000001.9:g.11230435_11230436del NCBI36
NG_033239.1:g.19762_19763del , LRG_734:g.19762_19763del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.1116+29_1116+30del ENSP00000515181.1:n.1116+29_1116+30del
ENST00000703132.1:n.1097+29_1097+30del
ENST00000703140.1:c.1116+29_1116+30del ENSP00000515197.1:n.1116+29_1116+30del
ENST00000703141.1:c.1116+29_1116+30del ENSP00000515198.1:n.1116+29_1116+30del
ENST00000703142.1:c.1116+29_1116+30del ENSP00000515199.1:n.1116+29_1116+30del
ENST00000703143.1:c.1116+29_1116+30del ENSP00000515200.1:n.1116+29_1116+30del
ENST00000703144.1:n.86+29_86+30del
ENST00000361445.9:c.1116+29_1116+30del MANE Select ENSP00000354558.4:n.1116+29_1116+30del
ENST00000361445.8:c.1116+29_1116+30del ENSP00000354558.4:n.1116+29_1116+30del
NM_004958.3:c.1116+29_1116+30del , LRG_734t1:c.1116+29_1116+30del NP_004949.1:n.1116+29_1116+30del
XM_005263438.1:c.1116+29_1116+30del XP_005263495.1:n.1116+29_1116+30del
XM_011541166.1:c.1116+29_1116+30del XP_011539468.1:n.1116+29_1116+30del
XR_244786.1:n.1237+29_1237+30del
XM_005263438.2:c.1116+29_1116+30del XP_005263495.1:n.1116+29_1116+30del
XM_011541166.2:c.1116+29_1116+30del XP_011539468.1:n.1116+29_1116+30del
XM_017000900.1:c.435+29_435+30del XP_016856389.1:n.435+29_435+30del
XM_017000901.1:c.-24+29_-24+30del XP_016856390.1:n.-24+29_-24+30del
XM_017000902.1:c.1116+29_1116+30del XP_016856391.1:n.1116+29_1116+30del
XM_024446187.1:c.1116+29_1116+30del XP_024301955.1:n.1116+29_1116+30del
XR_001737087.1:n.1237+29_1237+30del
NM_004958.4:c.1116+29_1116+30del MANE Select NP_004949.1:n.1116+29_1116+30del
NM_001386500.1:c.1116+29_1116+30del NP_001373429.1:n.1116+29_1116+30del
NM_001386501.1:c.-24+29_-24+30del NP_001373430.1:n.-24+29_-24+30del