Canonical Allele Identifier: CA1148438669
Gene: MTOR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11247991G= , CM000663.2:g.11247991G= GRCh38
NC_000001.10:g.11308048G= , CM000663.1:g.11308048G= GRCh37
NC_000001.9:g.11230635G= NCBI36
NG_033239.1:g.19561C= , LRG_734:g.19561C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.944C= ENSP00000515181.1:p.Pro315=
ENST00000703132.1:n.925C=
ENST00000703140.1:c.944C= ENSP00000515197.1:p.Pro315=
ENST00000703141.1:c.944C= ENSP00000515198.1:p.Pro315=
ENST00000703142.1:c.944C= ENSP00000515199.1:p.Pro315=
ENST00000703143.1:c.944C= ENSP00000515200.1:p.Pro315=
ENST00000361445.9:c.944C= MANE Select ENSP00000354558.4:p.Pro315=
ENST00000361445.8:c.944C= ENSP00000354558.4:p.Pro315=
NM_004958.3:c.944C= , LRG_734t1:c.944C= NP_004949.1:p.Pro315=
XM_005263438.1:c.944C= XP_005263495.1:p.Pro315=
XM_011541166.1:c.944C= XP_011539468.1:p.Pro315=
XR_244786.1:n.1065C=
XM_005263438.2:c.944C= XP_005263495.1:p.Pro315=
XM_011541166.2:c.944C= XP_011539468.1:p.Pro315=
XM_017000900.1:c.263C= XP_016856389.1:p.Pro88=
XM_017000901.1:c.-196C= XP_016856390.1:n.-196C=
XM_017000902.1:c.944C= XP_016856391.1:p.Pro315=
XM_024446187.1:c.944C= XP_024301955.1:p.Pro315=
XR_001737087.1:n.1065C=
NM_004958.4:c.944C= MANE Select NP_004949.1:p.Pro315=
NM_001386500.1:c.944C= NP_001373429.1:p.Pro315=
NM_001386501.1:c.-196C= NP_001373430.1:n.-196C=