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: CA1153539959
Community Standard Title: NM_004958.4(MTOR):c.6033+45G=
Gene: MTOR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11127959C= , CM000663.2:g.11127959C= GRCh38
NC_000001.10:g.11188016C= , CM000663.1:g.11188016C= GRCh37
NC_000001.9:g.11110603C= NCBI36
NG_033239.1:g.139593G= , LRG_734:g.139593G=

Transcript Alleles

HGVS Amino-acid Change
NM_004958.4:c.6033+45G= MANE Select NP_004949.1:n.6033+45G=
ENST00000361445.9:c.6033+45G= MANE Select ENSP00000354558.4:n.6033+45G=
NM_001386500.1:c.6033+45G= NP_001373429.1:n.6033+45G=
NM_001386501.1:c.4785+45G= NP_001373430.1:n.4785+45G=
NM_004958.3:c.6033+45G= , LRG_734t1:c.6033+45G= NP_004949.1:n.6033+45G=
ENST00000361445.8:c.6033+45G= ENSP00000354558.4:n.6033+45G=
ENST00000376838.5:c.648+45G= ENSP00000366034.1:n.648+45G=
ENST00000703118.1:c.*1408+45G= ENSP00000515181.1:n.*1408+45G=
ENST00000703131.1:n.1882G=
ENST00000703139.1:c.670+45G=
ENST00000703140.1:c.5820+45G= ENSP00000515197.1:n.5820+45G=
ENST00000703141.1:c.*1398G= ENSP00000515198.1:n.*1398G=
ENST00000703142.1:c.*2863+45G= ENSP00000515199.1:n.*2863+45G=
XM_005263438.1:c.6033+45G= XP_005263495.1:n.6033+45G=
XM_005263438.2:c.6033+45G= XP_005263495.1:n.6033+45G=
XM_017000900.1:c.5352+45G= XP_016856389.1:n.5352+45G=
XM_017000901.1:c.4785+45G= XP_016856390.1:n.4785+45G=
XM_024446187.1:c.6033+45G= XP_024301955.1:n.6033+45G=
XR_001737087.1:n.6154+45G=
XR_244786.1:n.6154+45G=
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