Canonical Allele Identifier: CA2742464399
Gene: MTOR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11247808_11247811del , CM000663.2:g.11247808_11247811del GRCh38
NC_000001.10:g.11307865_11307868del , CM000663.1:g.11307865_11307868del GRCh37
NC_000001.9:g.11230452_11230455del NCBI36
NG_033239.1:g.19742_19745del , LRG_734:g.19742_19745del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.1116+9_1116+12del ENSP00000515181.1:n.1116+9_1116+12del
ENST00000703132.1:n.1097+9_1097+12del
ENST00000703140.1:c.1116+9_1116+12del ENSP00000515197.1:n.1116+9_1116+12del
ENST00000703141.1:c.1116+9_1116+12del ENSP00000515198.1:n.1116+9_1116+12del
ENST00000703142.1:c.1116+9_1116+12del ENSP00000515199.1:n.1116+9_1116+12del
ENST00000703143.1:c.1116+9_1116+12del ENSP00000515200.1:n.1116+9_1116+12del
ENST00000703144.1:n.86+9_86+12del
ENST00000361445.9:c.1116+9_1116+12del MANE Select ENSP00000354558.4:n.1116+9_1116+12del
ENST00000361445.8:c.1116+9_1116+12del ENSP00000354558.4:n.1116+9_1116+12del
NM_004958.3:c.1116+9_1116+12del , LRG_734t1:c.1116+9_1116+12del NP_004949.1:n.1116+9_1116+12del
XM_005263438.1:c.1116+9_1116+12del XP_005263495.1:n.1116+9_1116+12del
XM_011541166.1:c.1116+9_1116+12del XP_011539468.1:n.1116+9_1116+12del
XR_244786.1:n.1237+9_1237+12del
XM_005263438.2:c.1116+9_1116+12del XP_005263495.1:n.1116+9_1116+12del
XM_011541166.2:c.1116+9_1116+12del XP_011539468.1:n.1116+9_1116+12del
XM_017000900.1:c.435+9_435+12del XP_016856389.1:n.435+9_435+12del
XM_017000901.1:c.-24+9_-24+12del XP_016856390.1:n.-24+9_-24+12del
XM_017000902.1:c.1116+9_1116+12del XP_016856391.1:n.1116+9_1116+12del
XM_024446187.1:c.1116+9_1116+12del XP_024301955.1:n.1116+9_1116+12del
XR_001737087.1:n.1237+9_1237+12del
NM_004958.4:c.1116+9_1116+12del MANE Select NP_004949.1:n.1116+9_1116+12del
NM_001386500.1:c.1116+9_1116+12del NP_001373429.1:n.1116+9_1116+12del
NM_001386501.1:c.-24+9_-24+12del NP_001373430.1:n.-24+9_-24+12del