Canonical Allele Identifier: CA1153540253

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11128126C= , CM000663.2:g.11128126C=	GRCh38
NC_000001.10:g.11188183C= , CM000663.1:g.11188183C=	GRCh37
NC_000001.9:g.11110770C=	NCBI36
NG_033239.1:g.139426G= , LRG_734:g.139426G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*1286G=	ENSP00000515181.1:n.*1286G=
ENST00000703131.1:n.1715G=
ENST00000703139.1:c.548G=
ENST00000703140.1:c.5698G=	ENSP00000515197.1:p.Ala1900=
ENST00000703141.1:c.*1231G=	ENSP00000515198.1:n.*1231G=
ENST00000703142.1:c.*2741G=	ENSP00000515199.1:n.*2741G=
ENST00000361445.9:c.5911G= MANE Select	ENSP00000354558.4:p.Ala1971=
ENST00000361445.8:c.5911G=	ENSP00000354558.4:p.Ala1971=
ENST00000376838.5:c.526G=	ENSP00000366034.1:p.Ala176=
NM_004958.3:c.5911G= , LRG_734t1:c.5911G=	NP_004949.1:p.Ala1971=
XM_005263438.1:c.5911G=	XP_005263495.1:p.Ala1971=
XR_244786.1:n.6032G=
XM_005263438.2:c.5911G=	XP_005263495.1:p.Ala1971=
XM_017000900.1:c.5230G=	XP_016856389.1:p.Ala1744=
XM_017000901.1:c.4663G=	XP_016856390.1:p.Ala1555=
XM_024446187.1:c.5911G=	XP_024301955.1:p.Ala1971=
XR_001737087.1:n.6032G=
NM_004958.4:c.5911G= MANE Select	NP_004949.1:p.Ala1971=
NM_001386500.1:c.5911G=	NP_001373429.1:p.Ala1971=
NM_001386501.1:c.4663G=	NP_001373430.1:p.Ala1555=