Canonical Allele Identifier: CA338400041
Gene: MTOR HGNC NCBI

Linked Data

ClinVar Variation Id: 2697093
ClinVar RCV Id: RCV003543796
dbSNP Id: rs2100940383
MyVariant Identifiers: chr1:g.11308016G>A (hg19) chr1:g.11247959G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11247959G>A , CM000663.2:g.11247959G>A GRCh38
NC_000001.10:g.11308016G>A , CM000663.1:g.11308016G>A GRCh37
NC_000001.9:g.11230603G>A NCBI36
NG_033239.1:g.19593C>T , LRG_734:g.19593C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.976C>T ENSP00000515181.1:p.Gln326Ter
ENST00000703132.1:n.957C>T
ENST00000703140.1:c.976C>T ENSP00000515197.1:p.Gln326Ter
ENST00000703141.1:c.976C>T ENSP00000515198.1:p.Gln326Ter
ENST00000703142.1:c.976C>T ENSP00000515199.1:p.Gln326Ter
ENST00000703143.1:c.976C>T ENSP00000515200.1:p.Gln326Ter
ENST00000361445.9:c.976C>T MANE Select ENSP00000354558.4:p.Gln326Ter
ENST00000361445.8:c.976C>T ENSP00000354558.4:p.Gln326Ter
NM_004958.3:c.976C>T , LRG_734t1:c.976C>T NP_004949.1:p.Gln326Ter
XM_005263438.1:c.976C>T XP_005263495.1:p.Gln326Ter
XM_011541166.1:c.976C>T XP_011539468.1:p.Gln326Ter
XR_244786.1:n.1097C>T
XM_005263438.2:c.976C>T XP_005263495.1:p.Gln326Ter
XM_011541166.2:c.976C>T XP_011539468.1:p.Gln326Ter
XM_017000900.1:c.295C>T XP_016856389.1:p.Gln99Ter
XM_017000901.1:c.-164C>T XP_016856390.1:n.-164C>T
XM_017000902.1:c.976C>T XP_016856391.1:p.Gln326Ter
XM_024446187.1:c.976C>T XP_024301955.1:p.Gln326Ter
XR_001737087.1:n.1097C>T
NM_004958.4:c.976C>T MANE Select NP_004949.1:p.Gln326Ter
NM_001386500.1:c.976C>T NP_001373429.1:p.Gln326Ter
NM_001386501.1:c.-164C>T NP_001373430.1:n.-164C>T
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