Canonical Allele Identifier: CA338399763
Gene: MTOR HGNC NCBI

Linked Data

ClinVar Variation Id: 1395602
ClinVar RCV Id: RCV001887211
dbSNP Id: rs1474925980
MyVariant Identifiers: chr1:g.11307963C>A (hg19) chr1:g.11247906C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11247906C>A , CM000663.2:g.11247906C>A GRCh38
NC_000001.10:g.11307963C>A , CM000663.1:g.11307963C>A GRCh37
NC_000001.9:g.11230550C>A NCBI36
NG_033239.1:g.19646G>T , LRG_734:g.19646G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000703118.1:c.1029G>T ENSP00000515181.1:p.Met343Ile
ENST00000703132.1:n.1010G>T
ENST00000703140.1:c.1029G>T ENSP00000515197.1:p.Met343Ile
ENST00000703141.1:c.1029G>T ENSP00000515198.1:p.Met343Ile
ENST00000703142.1:c.1029G>T ENSP00000515199.1:p.Met343Ile
ENST00000703143.1:c.1029G>T ENSP00000515200.1:p.Met343Ile
ENST00000361445.9:c.1029G>T MANE Select ENSP00000354558.4:p.Met343Ile
ENST00000361445.8:c.1029G>T ENSP00000354558.4:p.Met343Ile
NM_004958.3:c.1029G>T , LRG_734t1:c.1029G>T NP_004949.1:p.Met343Ile
XM_005263438.1:c.1029G>T XP_005263495.1:p.Met343Ile
XM_011541166.1:c.1029G>T XP_011539468.1:p.Met343Ile
XR_244786.1:n.1150G>T
XM_005263438.2:c.1029G>T XP_005263495.1:p.Met343Ile
XM_011541166.2:c.1029G>T XP_011539468.1:p.Met343Ile
XM_017000900.1:c.348G>T XP_016856389.1:p.Met116Ile
XM_017000901.1:c.-111G>T XP_016856390.1:n.-111G>T
XM_017000902.1:c.1029G>T XP_016856391.1:p.Met343Ile
XM_024446187.1:c.1029G>T XP_024301955.1:p.Met343Ile
XR_001737087.1:n.1150G>T
NM_004958.4:c.1029G>T MANE Select NP_004949.1:p.Met343Ile
NM_001386500.1:c.1029G>T NP_001373429.1:p.Met343Ile
NM_001386501.1:c.-111G>T NP_001373430.1:n.-111G>T
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