Canonical Allele Identifier: CA338400178
Gene: MTOR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.11308037A>C (hg19) chr1:g.11247980A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11247980A>C , CM000663.2:g.11247980A>C GRCh38
NC_000001.10:g.11308037A>C , CM000663.1:g.11308037A>C GRCh37
NC_000001.9:g.11230624A>C NCBI36
NG_033239.1:g.19572T>G , LRG_734:g.19572T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.955T>G ENSP00000515181.1:p.Phe319Val
ENST00000703132.1:n.936T>G
ENST00000703140.1:c.955T>G ENSP00000515197.1:p.Phe319Val
ENST00000703141.1:c.955T>G ENSP00000515198.1:p.Phe319Val
ENST00000703142.1:c.955T>G ENSP00000515199.1:p.Phe319Val
ENST00000703143.1:c.955T>G ENSP00000515200.1:p.Phe319Val
ENST00000361445.9:c.955T>G MANE Select ENSP00000354558.4:p.Phe319Val
ENST00000361445.8:c.955T>G ENSP00000354558.4:p.Phe319Val
NM_004958.3:c.955T>G , LRG_734t1:c.955T>G NP_004949.1:p.Phe319Val
XM_005263438.1:c.955T>G XP_005263495.1:p.Phe319Val
XM_011541166.1:c.955T>G XP_011539468.1:p.Phe319Val
XR_244786.1:n.1076T>G
XM_005263438.2:c.955T>G XP_005263495.1:p.Phe319Val
XM_011541166.2:c.955T>G XP_011539468.1:p.Phe319Val
XM_017000900.1:c.274T>G XP_016856389.1:p.Phe92Val
XM_017000901.1:c.-185T>G XP_016856390.1:n.-185T>G
XM_017000902.1:c.955T>G XP_016856391.1:p.Phe319Val
XM_024446187.1:c.955T>G XP_024301955.1:p.Phe319Val
XR_001737087.1:n.1076T>G
NM_004958.4:c.955T>G MANE Select NP_004949.1:p.Phe319Val
NM_001386500.1:c.955T>G NP_001373429.1:p.Phe319Val
NM_001386501.1:c.-185T>G NP_001373430.1:n.-185T>G
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