Canonical Allele Identifier: CA338399989
Gene: MTOR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.11308006G>T (hg19) chr1:g.11247949G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11247949G>T , CM000663.2:g.11247949G>T GRCh38
NC_000001.10:g.11308006G>T , CM000663.1:g.11308006G>T GRCh37
NC_000001.9:g.11230593G>T NCBI36
NG_033239.1:g.19603C>A , LRG_734:g.19603C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.986C>A ENSP00000515181.1:p.Ala329Asp
ENST00000703132.1:n.967C>A
ENST00000703140.1:c.986C>A ENSP00000515197.1:p.Ala329Asp
ENST00000703141.1:c.986C>A ENSP00000515198.1:p.Ala329Asp
ENST00000703142.1:c.986C>A ENSP00000515199.1:p.Ala329Asp
ENST00000703143.1:c.986C>A ENSP00000515200.1:p.Ala329Asp
ENST00000361445.9:c.986C>A MANE Select ENSP00000354558.4:p.Ala329Asp
ENST00000361445.8:c.986C>A ENSP00000354558.4:p.Ala329Asp
NM_004958.3:c.986C>A , LRG_734t1:c.986C>A NP_004949.1:p.Ala329Asp
XM_005263438.1:c.986C>A XP_005263495.1:p.Ala329Asp
XM_011541166.1:c.986C>A XP_011539468.1:p.Ala329Asp
XR_244786.1:n.1107C>A
XM_005263438.2:c.986C>A XP_005263495.1:p.Ala329Asp
XM_011541166.2:c.986C>A XP_011539468.1:p.Ala329Asp
XM_017000900.1:c.305C>A XP_016856389.1:p.Ala102Asp
XM_017000901.1:c.-154C>A XP_016856390.1:n.-154C>A
XM_017000902.1:c.986C>A XP_016856391.1:p.Ala329Asp
XM_024446187.1:c.986C>A XP_024301955.1:p.Ala329Asp
XR_001737087.1:n.1107C>A
NM_004958.4:c.986C>A MANE Select NP_004949.1:p.Ala329Asp
NM_001386500.1:c.986C>A NP_001373429.1:p.Ala329Asp
NM_001386501.1:c.-154C>A NP_001373430.1:n.-154C>A
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