Canonical Allele Identifier: CA338400014
Gene: MTOR HGNC NCBI

Linked Data

dbSNP Id: rs2100940363
MyVariant Identifiers: chr1:g.11308012G>C (hg19) chr1:g.11247955G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11247955G>C , CM000663.2:g.11247955G>C GRCh38
NC_000001.10:g.11308012G>C , CM000663.1:g.11308012G>C GRCh37
NC_000001.9:g.11230599G>C NCBI36
NG_033239.1:g.19597C>G , LRG_734:g.19597C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.980C>G ENSP00000515181.1:p.Ser327Ter
ENST00000703132.1:n.961C>G
ENST00000703140.1:c.980C>G ENSP00000515197.1:p.Ser327Ter
ENST00000703141.1:c.980C>G ENSP00000515198.1:p.Ser327Ter
ENST00000703142.1:c.980C>G ENSP00000515199.1:p.Ser327Ter
ENST00000703143.1:c.980C>G ENSP00000515200.1:p.Ser327Ter
ENST00000361445.9:c.980C>G MANE Select ENSP00000354558.4:p.Ser327Ter
ENST00000361445.8:c.980C>G ENSP00000354558.4:p.Ser327Ter
NM_004958.3:c.980C>G , LRG_734t1:c.980C>G NP_004949.1:p.Ser327Ter
XM_005263438.1:c.980C>G XP_005263495.1:p.Ser327Ter
XM_011541166.1:c.980C>G XP_011539468.1:p.Ser327Ter
XR_244786.1:n.1101C>G
XM_005263438.2:c.980C>G XP_005263495.1:p.Ser327Ter
XM_011541166.2:c.980C>G XP_011539468.1:p.Ser327Ter
XM_017000900.1:c.299C>G XP_016856389.1:p.Ser100Ter
XM_017000901.1:c.-160C>G XP_016856390.1:n.-160C>G
XM_017000902.1:c.980C>G XP_016856391.1:p.Ser327Ter
XM_024446187.1:c.980C>G XP_024301955.1:p.Ser327Ter
XR_001737087.1:n.1101C>G
NM_004958.4:c.980C>G MANE Select NP_004949.1:p.Ser327Ter
NM_001386500.1:c.980C>G NP_001373429.1:p.Ser327Ter
NM_001386501.1:c.-160C>G NP_001373430.1:n.-160C>G
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