Canonical Allele Identifier: CA1153502610

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109326T= , CM000663.2:g.11109326T=	GRCh38
NC_000001.10:g.11169383T= , CM000663.1:g.11169383T=	GRCh37
NC_000001.9:g.11091970T=	NCBI36
NG_033239.1:g.158226A= , LRG_734:g.158226A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2867A=	ENSP00000515181.1:n.*2867A=
ENST00000703131.1:n.3410A=
ENST00000703139.1:c.2280A=
ENST00000703140.1:c.7279A=	ENSP00000515197.1:p.Ile2427=
ENST00000703141.1:c.*3009A=	ENSP00000515198.1:n.*3009A=
ENST00000703142.1:c.*4322A=	ENSP00000515199.1:n.*4322A=
ENST00000361445.9:c.7492A= MANE Select	ENSP00000354558.4:p.Ile2498=
ENST00000361445.8:c.7492A=	ENSP00000354558.4:p.Ile2498=
ENST00000376838.5:c.2107A=	ENSP00000366034.1:p.Ile703=
ENST00000455339.1:c.460A=	ENSP00000398745.1:p.Ile154=
ENST00000473471.5:n.504A=
ENST00000490931.1:n.775A=
NM_004958.3:c.7492A= , LRG_734t1:c.7492A=	NP_004949.1:p.Ile2498=
XM_005263438.1:c.7492A=	XP_005263495.1:p.Ile2498=
XM_005263438.2:c.7492A=	XP_005263495.1:p.Ile2498=
XM_017000900.1:c.6811A=	XP_016856389.1:p.Ile2271=
XM_017000901.1:c.6244A=	XP_016856390.1:p.Ile2082=
XM_024446187.1:c.7492A=	XP_024301955.1:p.Ile2498=
XR_001737087.1:n.7530A=
NM_004958.4:c.7492A= MANE Select	NP_004949.1:p.Ile2498=
NM_001386500.1:c.7492A=	NP_001373429.1:p.Ile2498=
NM_001386501.1:c.6244A=	NP_001373430.1:p.Ile2082=