Canonical Allele Identifier: CA338400209
Gene: MTOR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.11308042G>C (hg19) chr1:g.11247985G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11247985G>C , CM000663.2:g.11247985G>C GRCh38
NC_000001.10:g.11308042G>C , CM000663.1:g.11308042G>C GRCh37
NC_000001.9:g.11230629G>C NCBI36
NG_033239.1:g.19567C>G , LRG_734:g.19567C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.950C>G ENSP00000515181.1:p.Thr317Ser
ENST00000703132.1:n.931C>G
ENST00000703140.1:c.950C>G ENSP00000515197.1:p.Thr317Ser
ENST00000703141.1:c.950C>G ENSP00000515198.1:p.Thr317Ser
ENST00000703142.1:c.950C>G ENSP00000515199.1:p.Thr317Ser
ENST00000703143.1:c.950C>G ENSP00000515200.1:p.Thr317Ser
ENST00000361445.9:c.950C>G MANE Select ENSP00000354558.4:p.Thr317Ser
ENST00000361445.8:c.950C>G ENSP00000354558.4:p.Thr317Ser
NM_004958.3:c.950C>G , LRG_734t1:c.950C>G NP_004949.1:p.Thr317Ser
XM_005263438.1:c.950C>G XP_005263495.1:p.Thr317Ser
XM_011541166.1:c.950C>G XP_011539468.1:p.Thr317Ser
XR_244786.1:n.1071C>G
XM_005263438.2:c.950C>G XP_005263495.1:p.Thr317Ser
XM_011541166.2:c.950C>G XP_011539468.1:p.Thr317Ser
XM_017000900.1:c.269C>G XP_016856389.1:p.Thr90Ser
XM_017000901.1:c.-190C>G XP_016856390.1:n.-190C>G
XM_017000902.1:c.950C>G XP_016856391.1:p.Thr317Ser
XM_024446187.1:c.950C>G XP_024301955.1:p.Thr317Ser
XR_001737087.1:n.1071C>G
NM_004958.4:c.950C>G MANE Select NP_004949.1:p.Thr317Ser
NM_001386500.1:c.950C>G NP_001373429.1:p.Thr317Ser
NM_001386501.1:c.-190C>G NP_001373430.1:n.-190C>G
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