Canonical Allele Identifier: CA589336
Gene: MTOR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11130657T>C , CM000663.2:g.11130657T>C GRCh38
NC_000001.10:g.11190714T>C , CM000663.1:g.11190714T>C GRCh37
NC_000001.9:g.11113301T>C NCBI36
NG_033239.1:g.136895A>G , LRG_734:g.136895A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.*860A>G ENSP00000515181.1:n.*860A>G
ENST00000703131.1:n.1289A>G
ENST00000703139.1:c.122A>G
ENST00000703140.1:c.5272A>G ENSP00000515197.1:p.Thr1758Ala
ENST00000703141.1:c.*805A>G ENSP00000515198.1:n.*805A>G
ENST00000703142.1:c.*2315A>G ENSP00000515199.1:n.*2315A>G
ENST00000361445.9:c.5485A>G MANE Select ENSP00000354558.4:p.Thr1829Ala
ENST00000361445.8:c.5485A>G ENSP00000354558.4:p.Thr1829Ala
ENST00000376838.5:c.100A>G ENSP00000366034.1:p.Thr34Ala
NM_004958.3:c.5485A>G , LRG_734t1:c.5485A>G NP_004949.1:p.Thr1829Ala
XM_005263438.1:c.5485A>G XP_005263495.1:p.Thr1829Ala
XR_244786.1:n.5606A>G
XM_005263438.2:c.5485A>G XP_005263495.1:p.Thr1829Ala
XM_017000900.1:c.4804A>G XP_016856389.1:p.Thr1602Ala
XM_017000901.1:c.4237A>G XP_016856390.1:p.Thr1413Ala
XM_024446187.1:c.5485A>G XP_024301955.1:p.Thr1829Ala
XR_001737087.1:n.5606A>G
NM_004958.4:c.5485A>G MANE Select NP_004949.1:p.Thr1829Ala
NM_001386500.1:c.5485A>G NP_001373429.1:p.Thr1829Ala
NM_001386501.1:c.4237A>G NP_001373430.1:p.Thr1413Ala
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