Canonical Allele Identifier: CA2573130659
Gene: MTOR HGNC NCBI

Linked Data

ClinVar Variation Id: 1484447
ClinVar RCV Id: RCV002005800
dbSNP Id: rs2100939628

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11247819del , CM000663.2:g.11247819del GRCh38
NC_000001.10:g.11307876del , CM000663.1:g.11307876del GRCh37
NC_000001.9:g.11230463del NCBI36
NG_033239.1:g.19734del , LRG_734:g.19734del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.1116+1del
ENST00000703132.1:n.1097+1del
ENST00000703140.1:c.1116+1del
ENST00000703141.1:c.1116+1del
ENST00000703142.1:c.1116+1del
ENST00000703143.1:c.1116+1del
ENST00000703144.1:n.86+1del
ENST00000361445.9:c.1116+1del
ENST00000361445.8:c.1116+1del
NM_004958.3:c.1116+1del , LRG_734t1:c.1116+1del
XM_005263438.1:c.1116+1del
XM_011541166.1:c.1116+1del
XR_244786.1:n.1237+1del
XM_005263438.2:c.1116+1del
XM_011541166.2:c.1116+1del
XM_017000900.1:c.435+1del
XM_017000901.1:c.-24+1del
XM_017000902.1:c.1116+1del
XM_024446187.1:c.1116+1del
XR_001737087.1:n.1237+1del
NM_004958.4:c.1116+1del
NM_001386500.1:c.1116+1del
NM_001386501.1:c.-24+1del