Canonical Allele Identifier: CA1153594860
Gene: MTOR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11247978G= , CM000663.2:g.11247978G= GRCh38
NC_000001.10:g.11308035G= , CM000663.1:g.11308035G= GRCh37
NC_000001.9:g.11230622G= NCBI36
NG_033239.1:g.19574C= , LRG_734:g.19574C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.957C= ENSP00000515181.1:p.Phe319=
ENST00000703132.1:n.938C=
ENST00000703140.1:c.957C= ENSP00000515197.1:p.Phe319=
ENST00000703141.1:c.957C= ENSP00000515198.1:p.Phe319=
ENST00000703142.1:c.957C= ENSP00000515199.1:p.Phe319=
ENST00000703143.1:c.957C= ENSP00000515200.1:p.Phe319=
ENST00000361445.9:c.957C= MANE Select ENSP00000354558.4:p.Phe319=
ENST00000361445.8:c.957C= ENSP00000354558.4:p.Phe319=
NM_004958.3:c.957C= , LRG_734t1:c.957C= NP_004949.1:p.Phe319=
XM_005263438.1:c.957C= XP_005263495.1:p.Phe319=
XM_011541166.1:c.957C= XP_011539468.1:p.Phe319=
XR_244786.1:n.1078C=
XM_005263438.2:c.957C= XP_005263495.1:p.Phe319=
XM_011541166.2:c.957C= XP_011539468.1:p.Phe319=
XM_017000900.1:c.276C= XP_016856389.1:p.Phe92=
XM_017000901.1:c.-183C= XP_016856390.1:n.-183C=
XM_017000902.1:c.957C= XP_016856391.1:p.Phe319=
XM_024446187.1:c.957C= XP_024301955.1:p.Phe319=
XR_001737087.1:n.1078C=
NM_004958.4:c.957C= MANE Select NP_004949.1:p.Phe319=
NM_001386500.1:c.957C= NP_001373429.1:p.Phe319=
NM_001386501.1:c.-183C= NP_001373430.1:n.-183C=