Canonical Allele Identifier: CA1153539816

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11127800C= , CM000663.2:g.11127800C=	GRCh38
NC_000001.10:g.11187857C= , CM000663.1:g.11187857C=	GRCh37
NC_000001.9:g.11110444C=	NCBI36
NG_033239.1:g.139752G= , LRG_734:g.139752G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*1415G=	ENSP00000515181.1:n.*1415G=
ENST00000703131.1:n.2041G=
ENST00000703139.1:c.677G=
ENST00000703140.1:c.5827G=	ENSP00000515197.1:p.Glu1943=
ENST00000703141.1:c.*1557G=	ENSP00000515198.1:n.*1557G=
ENST00000703142.1:c.*2870G=	ENSP00000515199.1:n.*2870G=
ENST00000361445.9:c.6040G= MANE Select	ENSP00000354558.4:p.Glu2014=
ENST00000361445.8:c.6040G=	ENSP00000354558.4:p.Glu2014=
ENST00000376838.5:c.655G=	ENSP00000366034.1:p.Glu219=
NM_004958.3:c.6040G= , LRG_734t1:c.6040G=	NP_004949.1:p.Glu2014=
XM_005263438.1:c.6040G=	XP_005263495.1:p.Glu2014=
XR_244786.1:n.6161G=
XM_005263438.2:c.6040G=	XP_005263495.1:p.Glu2014=
XM_017000900.1:c.5359G=	XP_016856389.1:p.Glu1787=
XM_017000901.1:c.4792G=	XP_016856390.1:p.Glu1598=
XM_024446187.1:c.6040G=	XP_024301955.1:p.Glu2014=
XR_001737087.1:n.6161G=
NM_004958.4:c.6040G= MANE Select	NP_004949.1:p.Glu2014=
NM_001386500.1:c.6040G=	NP_001373429.1:p.Glu2014=
NM_001386501.1:c.4792G=	NP_001373430.1:p.Glu1598=