Canonical Allele Identifier: CA2742464395
Gene: MTOR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11247796_11247797del , CM000663.2:g.11247796_11247797del GRCh38
NC_000001.10:g.11307853_11307854del , CM000663.1:g.11307853_11307854del GRCh37
NC_000001.9:g.11230440_11230441del NCBI36
NG_033239.1:g.19756_19757del , LRG_734:g.19756_19757del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.1116+23_1116+24del ENSP00000515181.1:n.1116+23_1116+24del
ENST00000703132.1:n.1097+23_1097+24del
ENST00000703140.1:c.1116+23_1116+24del ENSP00000515197.1:n.1116+23_1116+24del
ENST00000703141.1:c.1116+23_1116+24del ENSP00000515198.1:n.1116+23_1116+24del
ENST00000703142.1:c.1116+23_1116+24del ENSP00000515199.1:n.1116+23_1116+24del
ENST00000703143.1:c.1116+23_1116+24del ENSP00000515200.1:n.1116+23_1116+24del
ENST00000703144.1:n.86+23_86+24del
ENST00000361445.9:c.1116+23_1116+24del MANE Select ENSP00000354558.4:n.1116+23_1116+24del
ENST00000361445.8:c.1116+23_1116+24del ENSP00000354558.4:n.1116+23_1116+24del
NM_004958.3:c.1116+23_1116+24del , LRG_734t1:c.1116+23_1116+24del NP_004949.1:n.1116+23_1116+24del
XM_005263438.1:c.1116+23_1116+24del XP_005263495.1:n.1116+23_1116+24del
XM_011541166.1:c.1116+23_1116+24del XP_011539468.1:n.1116+23_1116+24del
XR_244786.1:n.1237+23_1237+24del
XM_005263438.2:c.1116+23_1116+24del XP_005263495.1:n.1116+23_1116+24del
XM_011541166.2:c.1116+23_1116+24del XP_011539468.1:n.1116+23_1116+24del
XM_017000900.1:c.435+23_435+24del XP_016856389.1:n.435+23_435+24del
XM_017000901.1:c.-24+23_-24+24del XP_016856390.1:n.-24+23_-24+24del
XM_017000902.1:c.1116+23_1116+24del XP_016856391.1:n.1116+23_1116+24del
XM_024446187.1:c.1116+23_1116+24del XP_024301955.1:n.1116+23_1116+24del
XR_001737087.1:n.1237+23_1237+24del
NM_004958.4:c.1116+23_1116+24del MANE Select NP_004949.1:n.1116+23_1116+24del
NM_001386500.1:c.1116+23_1116+24del NP_001373429.1:n.1116+23_1116+24del
NM_001386501.1:c.-24+23_-24+24del NP_001373430.1:n.-24+23_-24+24del