Canonical Allele Identifier: CA1153502824

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109408G= , CM000663.2:g.11109408G=	GRCh38
NC_000001.10:g.11169465G= , CM000663.1:g.11169465G=	GRCh37
NC_000001.9:g.11092052G=	NCBI36
NG_033239.1:g.158144C= , LRG_734:g.158144C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2823-38C=	ENSP00000515181.1:n.*2823-38C=
ENST00000703131.1:n.3366-38C=
ENST00000703139.1:c.2236-38C=
ENST00000703140.1:c.7235-38C=	ENSP00000515197.1:n.7235-38C=
ENST00000703141.1:c.*2965-38C=	ENSP00000515198.1:n.*2965-38C=
ENST00000703142.1:c.*4278-38C=	ENSP00000515199.1:n.*4278-38C=
ENST00000361445.9:c.7448-38C= MANE Select	ENSP00000354558.4:n.7448-38C=
ENST00000361445.8:c.7448-38C=	ENSP00000354558.4:n.7448-38C=
ENST00000376838.5:c.2063-38C=	ENSP00000366034.1:n.2063-38C=
ENST00000455339.1:c.416-38C=	ENSP00000398745.1:n.416-38C=
ENST00000473471.5:n.460-38C=
ENST00000490931.1:n.731-38C=
NM_004958.3:c.7448-38C= , LRG_734t1:c.7448-38C=	NP_004949.1:n.7448-38C=
XM_005263438.1:c.7448-38C=	XP_005263495.1:n.7448-38C=
XM_005263438.2:c.7448-38C=	XP_005263495.1:n.7448-38C=
XM_017000900.1:c.6767-38C=	XP_016856389.1:n.6767-38C=
XM_017000901.1:c.6200-38C=	XP_016856390.1:n.6200-38C=
XM_024446187.1:c.7448-38C=	XP_024301955.1:n.7448-38C=
XR_001737087.1:n.7486-38C=
NM_004958.4:c.7448-38C= MANE Select	NP_004949.1:n.7448-38C=
NM_001386500.1:c.7448-38C=	NP_001373429.1:n.7448-38C=
NM_001386501.1:c.6200-38C=	NP_001373430.1:n.6200-38C=