Canonical Allele Identifier: CA415916553
Gene: MTOR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.11169396T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11109339T>C , CM000663.2:g.11109339T>C GRCh38
NC_000001.10:g.11169396T>C , CM000663.1:g.11169396T>C GRCh37
NC_000001.9:g.11091983T>C NCBI36
NG_033239.1:g.158213A>G , LRG_734:g.158213A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.*2854A>G ENSP00000515181.1:n.*2854A>G
ENST00000703131.1:n.3397A>G
ENST00000703139.1:c.2267A>G
ENST00000703140.1:c.7266A>G ENSP00000515197.1:p.Leu2422=
ENST00000703141.1:c.*2996A>G ENSP00000515198.1:n.*2996A>G
ENST00000703142.1:c.*4309A>G ENSP00000515199.1:n.*4309A>G
ENST00000361445.9:c.7479A>G MANE Select ENSP00000354558.4:p.Leu2493=
ENST00000361445.8:c.7479A>G ENSP00000354558.4:p.Leu2493=
ENST00000376838.5:c.2094A>G ENSP00000366034.1:p.Leu698=
ENST00000455339.1:c.447A>G ENSP00000398745.1:p.Leu149=
ENST00000473471.5:n.491A>G
ENST00000490931.1:n.762A>G
NM_004958.3:c.7479A>G , LRG_734t1:c.7479A>G NP_004949.1:p.Leu2493=
XM_005263438.1:c.7479A>G XP_005263495.1:p.Leu2493=
XM_005263438.2:c.7479A>G XP_005263495.1:p.Leu2493=
XM_017000900.1:c.6798A>G XP_016856389.1:p.Leu2266=
XM_017000901.1:c.6231A>G XP_016856390.1:p.Leu2077=
XM_024446187.1:c.7479A>G XP_024301955.1:p.Leu2493=
XR_001737087.1:n.7517A>G
NM_004958.4:c.7479A>G MANE Select NP_004949.1:p.Leu2493=
NM_001386500.1:c.7479A>G NP_001373429.1:p.Leu2493=
NM_001386501.1:c.6231A>G NP_001373430.1:p.Leu2077=