Canonical Allele Identifier: CA338400647
Gene: MTOR HGNC NCBI

Linked Data

dbSNP Id: rs1194583768
gnomAD v2: 1-11308105-T-G
gnomAD v3: 1-11248048-T-G
gnomAD v4: 1-11248048-T-G
MyVariant Identifiers: chr1:g.11308105T>G (hg19) chr1:g.11248048T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11248048T>G , CM000663.2:g.11248048T>G GRCh38
NC_000001.10:g.11308105T>G , CM000663.1:g.11308105T>G GRCh37
NC_000001.9:g.11230692T>G NCBI36
NG_033239.1:g.19504A>C , LRG_734:g.19504A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.887A>C ENSP00000515181.1:p.His296Pro
ENST00000703132.1:n.868A>C
ENST00000703140.1:c.887A>C ENSP00000515197.1:p.His296Pro
ENST00000703141.1:c.887A>C ENSP00000515198.1:p.His296Pro
ENST00000703142.1:c.887A>C ENSP00000515199.1:p.His296Pro
ENST00000703143.1:c.887A>C ENSP00000515200.1:p.His296Pro
ENST00000361445.9:c.887A>C MANE Select ENSP00000354558.4:p.His296Pro
ENST00000361445.8:c.887A>C ENSP00000354558.4:p.His296Pro
NM_004958.3:c.887A>C , LRG_734t1:c.887A>C NP_004949.1:p.His296Pro
XM_005263438.1:c.887A>C XP_005263495.1:p.His296Pro
XM_011541166.1:c.887A>C XP_011539468.1:p.His296Pro
XR_244786.1:n.1008A>C
XM_005263438.2:c.887A>C XP_005263495.1:p.His296Pro
XM_011541166.2:c.887A>C XP_011539468.1:p.His296Pro
XM_017000900.1:c.206A>C XP_016856389.1:p.His69Pro
XM_017000901.1:c.-253A>C XP_016856390.1:n.-253A>C
XM_017000902.1:c.887A>C XP_016856391.1:p.His296Pro
XM_024446187.1:c.887A>C XP_024301955.1:p.His296Pro
XR_001737087.1:n.1008A>C
NM_004958.4:c.887A>C MANE Select NP_004949.1:p.His296Pro
NM_001386500.1:c.887A>C NP_001373429.1:p.His296Pro
NM_001386501.1:c.-253A>C NP_001373430.1:n.-253A>C
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