Canonical Allele Identifier: CA1153594909
Gene: MTOR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11247997A= , CM000663.2:g.11247997A= GRCh38
NC_000001.10:g.11308054A= , CM000663.1:g.11308054A= GRCh37
NC_000001.9:g.11230641A= NCBI36
NG_033239.1:g.19555T= , LRG_734:g.19555T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.938T= ENSP00000515181.1:p.Ile313=
ENST00000703132.1:n.919T=
ENST00000703140.1:c.938T= ENSP00000515197.1:p.Ile313=
ENST00000703141.1:c.938T= ENSP00000515198.1:p.Ile313=
ENST00000703142.1:c.938T= ENSP00000515199.1:p.Ile313=
ENST00000703143.1:c.938T= ENSP00000515200.1:p.Ile313=
ENST00000361445.9:c.938T= MANE Select ENSP00000354558.4:p.Ile313=
ENST00000361445.8:c.938T= ENSP00000354558.4:p.Ile313=
NM_004958.3:c.938T= , LRG_734t1:c.938T= NP_004949.1:p.Ile313=
XM_005263438.1:c.938T= XP_005263495.1:p.Ile313=
XM_011541166.1:c.938T= XP_011539468.1:p.Ile313=
XR_244786.1:n.1059T=
XM_005263438.2:c.938T= XP_005263495.1:p.Ile313=
XM_011541166.2:c.938T= XP_011539468.1:p.Ile313=
XM_017000900.1:c.257T= XP_016856389.1:p.Ile86=
XM_017000901.1:c.-202T= XP_016856390.1:n.-202T=
XM_017000902.1:c.938T= XP_016856391.1:p.Ile313=
XM_024446187.1:c.938T= XP_024301955.1:p.Ile313=
XR_001737087.1:n.1059T=
NM_004958.4:c.938T= MANE Select NP_004949.1:p.Ile313=
NM_001386500.1:c.938T= NP_001373429.1:p.Ile313=
NM_001386501.1:c.-202T= NP_001373430.1:n.-202T=