Canonical Allele Identifier: CA338378795

Gene: MTOR

Linked Data

• MyVariant Identifiers: chr1:g.11169425C>G (hg19) ; chr1:g.11109368C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109368C>G , CM000663.2:g.11109368C>G	GRCh38
NC_000001.10:g.11169425C>G , CM000663.1:g.11169425C>G	GRCh37
NC_000001.9:g.11092012C>G	NCBI36
NG_033239.1:g.158184G>C , LRG_734:g.158184G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2825G>C	ENSP00000515181.1:n.*2825G>C
ENST00000703131.1:n.3368G>C
ENST00000703139.1:c.2238G>C
ENST00000703140.1:c.7237G>C	ENSP00000515197.1:p.Gly2413Arg
ENST00000703141.1:c.*2967G>C	ENSP00000515198.1:n.*2967G>C
ENST00000703142.1:c.*4280G>C	ENSP00000515199.1:n.*4280G>C
ENST00000361445.9:c.7450G>C MANE Select	ENSP00000354558.4:p.Gly2484Arg
ENST00000361445.8:c.7450G>C	ENSP00000354558.4:p.Gly2484Arg
ENST00000376838.5:c.2065G>C	ENSP00000366034.1:p.Gly689Arg
ENST00000455339.1:c.418G>C	ENSP00000398745.1:p.Gly140Arg
ENST00000473471.5:n.462G>C
ENST00000490931.1:n.733G>C
NM_004958.3:c.7450G>C , LRG_734t1:c.7450G>C	NP_004949.1:p.Gly2484Arg
XM_005263438.1:c.7450G>C	XP_005263495.1:p.Gly2484Arg
XM_005263438.2:c.7450G>C	XP_005263495.1:p.Gly2484Arg
XM_017000900.1:c.6769G>C	XP_016856389.1:p.Gly2257Arg
XM_017000901.1:c.6202G>C	XP_016856390.1:p.Gly2068Arg
XM_024446187.1:c.7450G>C	XP_024301955.1:p.Gly2484Arg
XR_001737087.1:n.7488G>C
NM_004958.4:c.7450G>C MANE Select	NP_004949.1:p.Gly2484Arg
NM_001386500.1:c.7450G>C	NP_001373429.1:p.Gly2484Arg
NM_001386501.1:c.6202G>C	NP_001373430.1:p.Gly2068Arg