Canonical Allele Identifier: CA1143446847

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11248004G= , CM000663.2:g.11248004G=	GRCh38
NC_000001.10:g.11308061G= , CM000663.1:g.11308061G=	GRCh37
NC_000001.9:g.11230648G=	NCBI36
NG_033239.1:g.19548C= , LRG_734:g.19548C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.931C=	ENSP00000515181.1:p.Arg311=
ENST00000703132.1:n.912C=
ENST00000703140.1:c.931C=	ENSP00000515197.1:p.Arg311=
ENST00000703141.1:c.931C=	ENSP00000515198.1:p.Arg311=
ENST00000703142.1:c.931C=	ENSP00000515199.1:p.Arg311=
ENST00000703143.1:c.931C=	ENSP00000515200.1:p.Arg311=
ENST00000361445.9:c.931C= MANE Select	ENSP00000354558.4:p.Arg311=
ENST00000361445.8:c.931C=	ENSP00000354558.4:p.Arg311=
NM_004958.3:c.931C= , LRG_734t1:c.931C=	NP_004949.1:p.Arg311=
XM_005263438.1:c.931C=	XP_005263495.1:p.Arg311=
XM_011541166.1:c.931C=	XP_011539468.1:p.Arg311=
XR_244786.1:n.1052C=
XM_005263438.2:c.931C=	XP_005263495.1:p.Arg311=
XM_011541166.2:c.931C=	XP_011539468.1:p.Arg311=
XM_017000900.1:c.250C=	XP_016856389.1:p.Arg84=
XM_017000901.1:c.-209C=	XP_016856390.1:n.-209C=
XM_017000902.1:c.931C=	XP_016856391.1:p.Arg311=
XM_024446187.1:c.931C=	XP_024301955.1:p.Arg311=
XR_001737087.1:n.1052C=
NM_004958.4:c.931C= MANE Select	NP_004949.1:p.Arg311=
NM_001386500.1:c.931C=	NP_001373429.1:p.Arg311=
NM_001386501.1:c.-209C=	NP_001373430.1:n.-209C=