Canonical Allele Identifier: CA1153571242

Gene: MTOR

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11262099A>C , CM000663.2:g.11262099A>C	GRCh38
NC_000001.10:g.11322156A>C , CM000663.1:g.11322156A>C	GRCh37
NC_000001.9:g.11244743A>C	NCBI36
NG_033239.1:g.5453T>G , LRG_734:g.5453T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.-15+346T>G	ENSP00000515181.1:n.-15+346T>G
ENST00000703140.1:c.-15+346T>G	ENSP00000515197.1:n.-15+346T>G
ENST00000703141.1:c.-42+346T>G	ENSP00000515198.1:n.-42+346T>G
ENST00000703142.1:c.-15+346T>G	ENSP00000515199.1:n.-15+346T>G
ENST00000703143.1:c.-15+123T>G	ENSP00000515200.1:n.-15+123T>G
ENST00000361445.9:c.-15+346T>G MANE Select	ENSP00000354558.4:n.-15+346T>G
ENST00000361445.8:c.-15+346T>G	ENSP00000354558.4:n.-15+346T>G
NM_004958.3:c.-15+346T>G , LRG_734t1:c.-15+346T>G	NP_004949.1:n.-15+346T>G
XM_005263438.1:c.-42+346T>G	XP_005263495.1:n.-42+346T>G
XM_011541166.1:c.-15+346T>G	XP_011539468.1:n.-15+346T>G
XR_244786.1:n.107+346T>G
XM_005263438.2:c.-42+346T>G	XP_005263495.1:n.-42+346T>G
XM_011541166.2:c.-15+346T>G	XP_011539468.1:n.-15+346T>G
XM_017000902.1:c.-15+346T>G	XP_016856391.1:n.-15+346T>G
XM_024446187.1:c.-15+346T>G	XP_024301955.1:n.-15+346T>G
XR_001737087.1:n.107+346T>G
NM_004958.4:c.-15+346T>G MANE Select	NP_004949.1:n.-15+346T>G
NM_001386500.1:c.-42+346T>G	NP_001373429.1:n.-42+346T>G
NM_001386501.1:c.-1154+346T>G	NP_001373430.1:n.-1154+346T>G