Canonical Allele Identifier: CA338378592

Gene: MTOR

Linked Data

• MyVariant Identifiers: chr1:g.11169373A>C (hg19) ; chr1:g.11109316A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109316A>C , CM000663.2:g.11109316A>C	GRCh38
NC_000001.10:g.11169373A>C , CM000663.1:g.11169373A>C	GRCh37
NC_000001.9:g.11091960A>C	NCBI36
NG_033239.1:g.158236T>G , LRG_734:g.158236T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2877T>G	ENSP00000515181.1:n.*2877T>G
ENST00000703131.1:n.3420T>G
ENST00000703139.1:c.2290T>G
ENST00000703140.1:c.7289T>G	ENSP00000515197.1:p.Ile2430Ser
ENST00000703141.1:c.*3019T>G	ENSP00000515198.1:n.*3019T>G
ENST00000703142.1:c.*4332T>G	ENSP00000515199.1:n.*4332T>G
ENST00000361445.9:c.7502T>G MANE Select	ENSP00000354558.4:p.Ile2501Ser
ENST00000361445.8:c.7502T>G	ENSP00000354558.4:p.Ile2501Ser
ENST00000376838.5:c.2117T>G	ENSP00000366034.1:p.Ile706Ser
ENST00000455339.1:c.470T>G	ENSP00000398745.1:p.Ile157Ser
ENST00000473471.5:n.514T>G
ENST00000490931.1:n.785T>G
NM_004958.3:c.7502T>G , LRG_734t1:c.7502T>G	NP_004949.1:p.Ile2501Ser
XM_005263438.1:c.7502T>G	XP_005263495.1:p.Ile2501Ser
XM_005263438.2:c.7502T>G	XP_005263495.1:p.Ile2501Ser
XM_017000900.1:c.6821T>G	XP_016856389.1:p.Ile2274Ser
XM_017000901.1:c.6254T>G	XP_016856390.1:p.Ile2085Ser
XM_024446187.1:c.7502T>G	XP_024301955.1:p.Ile2501Ser
XR_001737087.1:n.7540T>G
NM_004958.4:c.7502T>G MANE Select	NP_004949.1:p.Ile2501Ser
NM_001386500.1:c.7502T>G	NP_001373429.1:p.Ile2501Ser
NM_001386501.1:c.6254T>G	NP_001373430.1:p.Ile2085Ser