Canonical Allele Identifier: CA1153514352

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11114326A= , CM000663.2:g.11114326A=	GRCh38
NC_000001.10:g.11174383A= , CM000663.1:g.11174383A=	GRCh37
NC_000001.9:g.11096970A=	NCBI36
NG_033239.1:g.153226T= , LRG_734:g.153226T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2667T=	ENSP00000515181.1:n.*2667T=
ENST00000703131.1:n.3210T=
ENST00000703139.1:c.2080T=
ENST00000703140.1:c.7079T=	ENSP00000515197.1:p.Leu2360=
ENST00000703141.1:c.*2809T=	ENSP00000515198.1:n.*2809T=
ENST00000703142.1:c.*4122T=	ENSP00000515199.1:n.*4122T=
ENST00000361445.9:c.7292T= MANE Select	ENSP00000354558.4:p.Leu2431=
ENST00000361445.8:c.7292T=	ENSP00000354558.4:p.Leu2431=
ENST00000376838.5:c.1907T=	ENSP00000366034.1:p.Leu636=
ENST00000455339.1:c.260T=	ENSP00000398745.1:p.Leu87=
ENST00000473471.5:n.304T=
ENST00000490931.1:n.335T=
NM_004958.3:c.7292T= , LRG_734t1:c.7292T=	NP_004949.1:p.Leu2431=
XM_005263438.1:c.7292T=	XP_005263495.1:p.Leu2431=
XR_244786.1:n.7330T=
XM_005263438.2:c.7292T=	XP_005263495.1:p.Leu2431=
XM_017000900.1:c.6611T=	XP_016856389.1:p.Leu2204=
XM_017000901.1:c.6044T=	XP_016856390.1:p.Leu2015=
XM_024446187.1:c.7292T=	XP_024301955.1:p.Leu2431=
XR_001737087.1:n.7330T=
NM_004958.4:c.7292T= MANE Select	NP_004949.1:p.Leu2431=
NM_001386500.1:c.7292T=	NP_001373429.1:p.Leu2431=
NM_001386501.1:c.6044T=	NP_001373430.1:p.Leu2015=