Canonical Allele Identifier: CA588941

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11115387T>C , CM000663.2:g.11115387T>C	GRCh38
NC_000001.10:g.11175444T>C , CM000663.1:g.11175444T>C	GRCh37
NC_000001.9:g.11098031T>C	NCBI36
NG_033239.1:g.152165A>G , LRG_734:g.152165A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004958.4:c.7089+9A>G MANE Select	NP_004949.1:n.7089+9A>G
ENST00000361445.9:c.7089+9A>G MANE Select	ENSP00000354558.4:n.7089+9A>G
NM_001386500.1:c.7089+9A>G	NP_001373429.1:n.7089+9A>G
NM_001386501.1:c.5841+9A>G	NP_001373430.1:n.5841+9A>G
NM_004958.3:c.7089+9A>G , LRG_734t1:c.7089+9A>G	NP_004949.1:n.7089+9A>G
ENST00000361445.8:c.7089+9A>G	ENSP00000354558.4:n.7089+9A>G
ENST00000376838.5:c.1704+9A>G	ENSP00000366034.1:n.1704+9A>G
ENST00000455339.1:c.57+9A>G	ENSP00000398745.1:n.57+9A>G
ENST00000490931.1:n.132+9A>G
ENST00000703118.1:c.*2464+9A>G	ENSP00000515181.1:n.*2464+9A>G
ENST00000703131.1:n.3007+9A>G
ENST00000703139.1:c.1877+9A>G
ENST00000703140.1:c.6876+9A>G	ENSP00000515197.1:n.6876+9A>G
ENST00000703141.1:c.*2606+9A>G	ENSP00000515198.1:n.*2606+9A>G
ENST00000703142.1:c.*3919+9A>G	ENSP00000515199.1:n.*3919+9A>G
XM_005263438.1:c.7089+9A>G	XP_005263495.1:n.7089+9A>G
XM_005263438.2:c.7089+9A>G	XP_005263495.1:n.7089+9A>G
XM_017000900.1:c.6408+9A>G	XP_016856389.1:n.6408+9A>G
XM_017000901.1:c.5841+9A>G	XP_016856390.1:n.5841+9A>G
XM_024446187.1:c.7089+9A>G	XP_024301955.1:n.7089+9A>G
XR_001737087.1:n.7127+9A>G
XR_244786.1:n.7127+9A>G