Canonical Allele Identifier: CA415916543

Gene: MTOR

Linked Data

• MyVariant Identifiers: chr1:g.11169384A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109327A>C , CM000663.2:g.11109327A>C	GRCh38
NC_000001.10:g.11169384A>C , CM000663.1:g.11169384A>C	GRCh37
NC_000001.9:g.11091971A>C	NCBI36
NG_033239.1:g.158225T>G , LRG_734:g.158225T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2866T>G	ENSP00000515181.1:n.*2866T>G
ENST00000703131.1:n.3409T>G
ENST00000703139.1:c.2279T>G
ENST00000703140.1:c.7278T>G	ENSP00000515197.1:p.Ala2426=
ENST00000703141.1:c.*3008T>G	ENSP00000515198.1:n.*3008T>G
ENST00000703142.1:c.*4321T>G	ENSP00000515199.1:n.*4321T>G
ENST00000361445.9:c.7491T>G MANE Select	ENSP00000354558.4:p.Ala2497=
ENST00000361445.8:c.7491T>G	ENSP00000354558.4:p.Ala2497=
ENST00000376838.5:c.2106T>G	ENSP00000366034.1:p.Ala702=
ENST00000455339.1:c.459T>G	ENSP00000398745.1:p.Ala153=
ENST00000473471.5:n.503T>G
ENST00000490931.1:n.774T>G
NM_004958.3:c.7491T>G , LRG_734t1:c.7491T>G	NP_004949.1:p.Ala2497=
XM_005263438.1:c.7491T>G	XP_005263495.1:p.Ala2497=
XM_005263438.2:c.7491T>G	XP_005263495.1:p.Ala2497=
XM_017000900.1:c.6810T>G	XP_016856389.1:p.Ala2270=
XM_017000901.1:c.6243T>G	XP_016856390.1:p.Ala2081=
XM_024446187.1:c.7491T>G	XP_024301955.1:p.Ala2497=
XR_001737087.1:n.7529T>G
NM_004958.4:c.7491T>G MANE Select	NP_004949.1:p.Ala2497=
NM_001386500.1:c.7491T>G	NP_001373429.1:p.Ala2497=
NM_001386501.1:c.6243T>G	NP_001373430.1:p.Ala2081=