Canonical Allele Identifier: CA338372140

Gene: MTOR

Linked Data

• dbSNP Id: rs2100568440
• MyVariant Identifiers: chr1:g.11217325C>G (hg19) ; chr1:g.11157268C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11157268C>G , CM000663.2:g.11157268C>G	GRCh38
NC_000001.10:g.11217325C>G , CM000663.1:g.11217325C>G	GRCh37
NC_000001.9:g.11139912C>G	NCBI36
NG_033239.1:g.110284G>C , LRG_734:g.110284G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.4353G>C	ENSP00000515181.1:p.Glu1451Asp
ENST00000703131.1:n.273G>C
ENST00000703140.1:c.4140G>C	ENSP00000515197.1:p.Glu1380Asp
ENST00000703141.1:c.4353G>C	ENSP00000515198.1:p.Glu1451Asp
ENST00000703142.1:c.*1183G>C	ENSP00000515199.1:n.*1183G>C
ENST00000361445.9:c.4353G>C MANE Select	ENSP00000354558.4:p.Glu1451Asp
ENST00000361445.8:c.4353G>C	ENSP00000354558.4:p.Glu1451Asp
NM_004958.3:c.4353G>C , LRG_734t1:c.4353G>C	NP_004949.1:p.Glu1451Asp
XM_005263438.1:c.4353G>C	XP_005263495.1:p.Glu1451Asp
XM_011541166.1:c.4353G>C	XP_011539468.1:p.Glu1451Asp
XR_244786.1:n.4474G>C
XM_005263438.2:c.4353G>C	XP_005263495.1:p.Glu1451Asp
XM_011541166.2:c.4353G>C	XP_011539468.1:p.Glu1451Asp
XM_017000900.1:c.3672G>C	XP_016856389.1:p.Glu1224Asp
XM_017000901.1:c.3105G>C	XP_016856390.1:p.Glu1035Asp
XM_024446187.1:c.4353G>C	XP_024301955.1:p.Glu1451Asp
XR_001737087.1:n.4474G>C
NM_004958.4:c.4353G>C MANE Select	NP_004949.1:p.Glu1451Asp
NM_001386500.1:c.4353G>C	NP_001373429.1:p.Glu1451Asp
NM_001386501.1:c.3105G>C	NP_001373430.1:p.Glu1035Asp