Canonical Allele Identifier: CA416041946
Gene: MTOR HGNC NCBI

Linked Data

COSMIC: COSM1579061
MyVariant Identifiers: chr1:g.11307987del (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11247933del , CM000663.2:g.11247933del GRCh38
NC_000001.10:g.11307990del , CM000663.1:g.11307990del GRCh37
NC_000001.9:g.11230577del NCBI36
NG_033239.1:g.19622del , LRG_734:g.19622del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.1005del ENSP00000515181.1:p.Tyr336ThrfsTer?
ENST00000703132.1:n.986del
ENST00000703140.1:c.1005del ENSP00000515197.1:p.Tyr336ThrfsTer?
ENST00000703141.1:c.1005del ENSP00000515198.1:p.Tyr336ThrfsTer?
ENST00000703142.1:c.1005del ENSP00000515199.1:p.Tyr336ThrfsTer?
ENST00000703143.1:c.1005del ENSP00000515200.1:p.Tyr336ThrfsTer?
ENST00000361445.9:c.1005del MANE Select ENSP00000354558.4:p.Tyr336ThrfsTer?
ENST00000361445.8:c.1005del ENSP00000354558.4:p.Tyr336ThrfsTer?
NM_004958.3:c.1005del , LRG_734t1:c.1005del NP_004949.1:p.Tyr336ThrfsTer?
XM_005263438.1:c.1005del XP_005263495.1:p.Tyr336ThrfsTer?
XM_011541166.1:c.1005del XP_011539468.1:p.Tyr336ThrfsTer?
XR_244786.1:n.1126del
XM_005263438.2:c.1005del XP_005263495.1:p.Tyr336ThrfsTer?
XM_011541166.2:c.1005del XP_011539468.1:p.Tyr336ThrfsTer?
XM_017000900.1:c.324del XP_016856389.1:p.Tyr109ThrfsTer?
XM_017000901.1:c.-135del XP_016856390.1:n.-135del
XM_017000902.1:c.1005del XP_016856391.1:p.Tyr336ThrfsTer?
XM_024446187.1:c.1005del XP_024301955.1:p.Tyr336ThrfsTer?
XR_001737087.1:n.1126del
NM_004958.4:c.1005del MANE Select NP_004949.1:p.Tyr336ThrfsTer?
NM_001386500.1:c.1005del NP_001373429.1:p.Tyr336ThrfsTer?
NM_001386501.1:c.-135del NP_001373430.1:n.-135del
Search 100 bp 5'
Search 100 bp 3'