Canonical Allele Identifier: CA1153502625

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109357C= , CM000663.2:g.11109357C=	GRCh38
NC_000001.10:g.11169414C= , CM000663.1:g.11169414C=	GRCh37
NC_000001.9:g.11092001C=	NCBI36
NG_033239.1:g.158195G= , LRG_734:g.158195G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2836G=	ENSP00000515181.1:n.*2836G=
ENST00000703131.1:n.3379G=
ENST00000703139.1:c.2249G=
ENST00000703140.1:c.7248G=	ENSP00000515197.1:p.Leu2416=
ENST00000703141.1:c.*2978G=	ENSP00000515198.1:n.*2978G=
ENST00000703142.1:c.*4291G=	ENSP00000515199.1:n.*4291G=
ENST00000361445.9:c.7461G= MANE Select	ENSP00000354558.4:p.Leu2487=
ENST00000361445.8:c.7461G=	ENSP00000354558.4:p.Leu2487=
ENST00000376838.5:c.2076G=	ENSP00000366034.1:p.Leu692=
ENST00000455339.1:c.429G=	ENSP00000398745.1:p.Leu143=
ENST00000473471.5:n.473G=
ENST00000490931.1:n.744G=
NM_004958.3:c.7461G= , LRG_734t1:c.7461G=	NP_004949.1:p.Leu2487=
XM_005263438.1:c.7461G=	XP_005263495.1:p.Leu2487=
XM_005263438.2:c.7461G=	XP_005263495.1:p.Leu2487=
XM_017000900.1:c.6780G=	XP_016856389.1:p.Leu2260=
XM_017000901.1:c.6213G=	XP_016856390.1:p.Leu2071=
XM_024446187.1:c.7461G=	XP_024301955.1:p.Leu2487=
XR_001737087.1:n.7499G=
NM_004958.4:c.7461G= MANE Select	NP_004949.1:p.Leu2487=
NM_001386500.1:c.7461G=	NP_001373429.1:p.Leu2487=
NM_001386501.1:c.6213G=	NP_001373430.1:p.Leu2071=