Canonical Allele Identifier: CA1153543792

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11130747C= , CM000663.2:g.11130747C=	GRCh38
NC_000001.10:g.11190804C= , CM000663.1:g.11190804C=	GRCh37
NC_000001.9:g.11113391C=	NCBI36
NG_033239.1:g.136805G= , LRG_734:g.136805G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004958.4:c.5395G= MANE Select	NP_004949.1:p.Glu1799=
ENST00000361445.9:c.5395G= MANE Select	ENSP00000354558.4:p.Glu1799=
NM_001386500.1:c.5395G=	NP_001373429.1:p.Glu1799=
NM_001386501.1:c.4147G=	NP_001373430.1:p.Glu1383=
NM_004958.3:c.5395G= , LRG_734t1:c.5395G=	NP_004949.1:p.Glu1799=
ENST00000361445.8:c.5395G=	ENSP00000354558.4:p.Glu1799=
ENST00000376838.5:c.10G=	ENSP00000366034.1:p.Glu4=
ENST00000703118.1:c.*770G=	ENSP00000515181.1:n.*770G=
ENST00000703131.1:n.1199G=
ENST00000703139.1:c.32G=
ENST00000703140.1:c.5182G=	ENSP00000515197.1:p.Glu1728=
ENST00000703141.1:c.*715G=	ENSP00000515198.1:n.*715G=
ENST00000703142.1:c.*2225G=	ENSP00000515199.1:n.*2225G=
XM_005263438.1:c.5395G=	XP_005263495.1:p.Glu1799=
XM_005263438.2:c.5395G=	XP_005263495.1:p.Glu1799=
XM_017000900.1:c.4714G=	XP_016856389.1:p.Glu1572=
XM_017000901.1:c.4147G=	XP_016856390.1:p.Glu1383=
XM_024446187.1:c.5395G=	XP_024301955.1:p.Glu1799=
XR_001737087.1:n.5516G=
XR_244786.1:n.5516G=