Canonical Allele Identifier: CA1139898446

Gene: MTOR

Genomic Alleles

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

Transcript Alleles

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