Canonical Allele Identifier: CA1153502479
Gene: MTOR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11109228C= , CM000663.2:g.11109228C= GRCh38
NC_000001.10:g.11169285C= , CM000663.1:g.11169285C= GRCh37
NC_000001.9:g.11091872C= NCBI36
NG_033239.1:g.158324G= , LRG_734:g.158324G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.*2903+62G= ENSP00000515181.1:n.*2903+62G=
ENST00000703131.1:n.3446+62G=
ENST00000703139.1:c.2316+62G=
ENST00000703140.1:c.7315+62G= ENSP00000515197.1:n.7315+62G=
ENST00000703141.1:c.*3045+62G= ENSP00000515198.1:n.*3045+62G=
ENST00000703142.1:c.*4358+62G= ENSP00000515199.1:n.*4358+62G=
ENST00000361445.9:c.7528+62G= MANE Select ENSP00000354558.4:n.7528+62G=
ENST00000361445.8:c.7528+62G= ENSP00000354558.4:n.7528+62G=
ENST00000376838.5:c.2143+62G= ENSP00000366034.1:n.2143+62G=
ENST00000473471.5:n.540+62G=
ENST00000490931.1:n.811+62G=
NM_004958.3:c.7528+62G= , LRG_734t1:c.7528+62G= NP_004949.1:n.7528+62G=
XM_005263438.1:c.7528+62G= XP_005263495.1:n.7528+62G=
XM_005263438.2:c.7528+62G= XP_005263495.1:n.7528+62G=
XM_017000900.1:c.6847+62G= XP_016856389.1:n.6847+62G=
XM_017000901.1:c.6280+62G= XP_016856390.1:n.6280+62G=
XM_024446187.1:c.7528+62G= XP_024301955.1:n.7528+62G=
XR_001737087.1:n.7566+62G=
NM_004958.4:c.7528+62G= MANE Select NP_004949.1:n.7528+62G=
NM_001386500.1:c.7528+62G= NP_001373429.1:n.7528+62G=
NM_001386501.1:c.6280+62G= NP_001373430.1:n.6280+62G=