Canonical Allele Identifier: CA1153537820
Gene: MTOR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11157184G= , CM000663.2:g.11157184G= GRCh38
NC_000001.10:g.11217241G= , CM000663.1:g.11217241G= GRCh37
NC_000001.9:g.11139828G= NCBI36
NG_033239.1:g.110368C= , LRG_734:g.110368C=

Transcript Alleles

HGVS Amino-acid change
ENST00000703118.1:c.4437C= ENSP00000515181.1:p.Gly1479=
ENST00000703131.1:n.357C=
ENST00000703140.1:c.4224C= ENSP00000515197.1:p.Gly1408=
ENST00000703141.1:c.4437C= ENSP00000515198.1:p.Gly1479=
ENST00000703142.1:c.*1267C= ENSP00000515199.1:n.*1267C=
ENST00000361445.9:c.4437C= MANE Select ENSP00000354558.4:p.Gly1479=
ENST00000361445.8:c.4437C= ENSP00000354558.4:p.Gly1479=
NM_004958.3:c.4437C= , LRG_734t1:c.4437C= NP_004949.1:p.Gly1479=
XM_005263438.1:c.4437C= XP_005263495.1:p.Gly1479=
XM_011541166.1:c.4437C= XP_011539468.1:p.Gly1479=
XR_244786.1:n.4558C=
XM_005263438.2:c.4437C= XP_005263495.1:p.Gly1479=
XM_011541166.2:c.4437C= XP_011539468.1:p.Gly1479=
XM_017000900.1:c.3756C= XP_016856389.1:p.Gly1252=
XM_017000901.1:c.3189C= XP_016856390.1:p.Gly1063=
XM_024446187.1:c.4437C= XP_024301955.1:p.Gly1479=
XR_001737087.1:n.4558C=
NM_004958.4:c.4437C= MANE Select NP_004949.1:p.Gly1479=
NM_001386500.1:c.4437C= NP_001373429.1:p.Gly1479=
NM_001386501.1:c.3189C= NP_001373430.1:p.Gly1063=