Canonical Allele Identifier: CA1139927278

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11262508C= , CM000663.2:g.11262508C=	GRCh38
NC_000001.10:g.11322565C= , CM000663.1:g.11322565C=	GRCh37
NC_000001.9:g.11245152C=	NCBI36
NG_033239.1:g.5044G= , LRG_734:g.5044G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004958.4:c.-78G= MANE Select	NP_004949.1:n.-78G=
ENST00000361445.9:c.-78G= MANE Select	ENSP00000354558.4:n.-78G=
NM_001386500.1:c.-105G=	NP_001373429.1:n.-105G=
NM_001386501.1:c.-1217G=	NP_001373430.1:n.-1217G=
NM_004958.3:c.-78G= , LRG_734t1:c.-78G=	NP_004949.1:n.-78G=
ENST00000703118.1:c.-78G=	ENSP00000515181.1:n.-78G=
ENST00000703140.1:c.-78G=	ENSP00000515197.1:n.-78G=
ENST00000703141.1:c.-105G=	ENSP00000515198.1:n.-105G=
ENST00000703142.1:c.-78G=	ENSP00000515199.1:n.-78G=
ENST00000703143.1:c.-301G=	ENSP00000515200.1:n.-301G=
XM_005263438.1:c.-105G=	XP_005263495.1:n.-105G=
XM_005263438.2:c.-105G=	XP_005263495.1:n.-105G=
XM_011541166.1:c.-78G=	XP_011539468.1:n.-78G=
XM_011541166.2:c.-78G=	XP_011539468.1:n.-78G=
XM_017000902.1:c.-78G=	XP_016856391.1:n.-78G=
XM_024446187.1:c.-78G=	XP_024301955.1:n.-78G=
XR_001737087.1:n.44G=
XR_244786.1:n.44G=