This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: CA1149138170
Gene: MTOR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11128072T= , CM000663.2:g.11128072T= GRCh38
NC_000001.10:g.11188129T= , CM000663.1:g.11188129T= GRCh37
NC_000001.9:g.11110716T= NCBI36
NG_033239.1:g.139480A= , LRG_734:g.139480A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.*1340A= ENSP00000515181.1:n.*1340A=
ENST00000703131.1:n.1769A=
ENST00000703139.1:c.602A=
ENST00000703140.1:c.5752A= ENSP00000515197.1:p.Asn1918=
ENST00000703141.1:c.*1285A= ENSP00000515198.1:n.*1285A=
ENST00000703142.1:c.*2795A= ENSP00000515199.1:n.*2795A=
ENST00000361445.9:c.5965A= MANE Select ENSP00000354558.4:p.Asn1989=
ENST00000361445.8:c.5965A= ENSP00000354558.4:p.Asn1989=
ENST00000376838.5:c.580A= ENSP00000366034.1:p.Asn194=
NM_004958.3:c.5965A= , LRG_734t1:c.5965A= NP_004949.1:p.Asn1989=
XM_005263438.1:c.5965A= XP_005263495.1:p.Asn1989=
XR_244786.1:n.6086A=
XM_005263438.2:c.5965A= XP_005263495.1:p.Asn1989=
XM_017000900.1:c.5284A= XP_016856389.1:p.Asn1762=
XM_017000901.1:c.4717A= XP_016856390.1:p.Asn1573=
XM_024446187.1:c.5965A= XP_024301955.1:p.Asn1989=
XR_001737087.1:n.6086A=
NM_004958.4:c.5965A= MANE Select NP_004949.1:p.Asn1989=
NM_001386500.1:c.5965A= NP_001373429.1:p.Asn1989=
NM_001386501.1:c.4717A= NP_001373430.1:p.Asn1573=
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