Canonical Allele Identifier: CA1153502592

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109320T= , CM000663.2:g.11109320T=	GRCh38
NC_000001.10:g.11169377T= , CM000663.1:g.11169377T=	GRCh37
NC_000001.9:g.11091964T=	NCBI36
NG_033239.1:g.158232A= , LRG_734:g.158232A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2873A=	ENSP00000515181.1:n.*2873A=
ENST00000703131.1:n.3416A=
ENST00000703139.1:c.2286A=
ENST00000703140.1:c.7285A=	ENSP00000515197.1:p.Ile2429=
ENST00000703141.1:c.*3015A=	ENSP00000515198.1:n.*3015A=
ENST00000703142.1:c.*4328A=	ENSP00000515199.1:n.*4328A=
ENST00000361445.9:c.7498A= MANE Select	ENSP00000354558.4:p.Ile2500=
ENST00000361445.8:c.7498A=	ENSP00000354558.4:p.Ile2500=
ENST00000376838.5:c.2113A=	ENSP00000366034.1:p.Ile705=
ENST00000455339.1:c.466A=	ENSP00000398745.1:p.Ile156=
ENST00000473471.5:n.510A=
ENST00000490931.1:n.781A=
NM_004958.3:c.7498A= , LRG_734t1:c.7498A=	NP_004949.1:p.Ile2500=
XM_005263438.1:c.7498A=	XP_005263495.1:p.Ile2500=
XM_005263438.2:c.7498A=	XP_005263495.1:p.Ile2500=
XM_017000900.1:c.6817A=	XP_016856389.1:p.Ile2273=
XM_017000901.1:c.6250A=	XP_016856390.1:p.Ile2084=
XM_024446187.1:c.7498A=	XP_024301955.1:p.Ile2500=
XR_001737087.1:n.7536A=
NM_004958.4:c.7498A= MANE Select	NP_004949.1:p.Ile2500=
NM_001386500.1:c.7498A=	NP_001373429.1:p.Ile2500=
NM_001386501.1:c.6250A=	NP_001373430.1:p.Ile2084=