Canonical Allele Identifier: CA338398803

Gene: MTOR

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11130747C>G , CM000663.2:g.11130747C>G	GRCh38
NC_000001.10:g.11190804C>G , CM000663.1:g.11190804C>G	GRCh37
NC_000001.9:g.11113391C>G	NCBI36
NG_033239.1:g.136805G>C , LRG_734:g.136805G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*770G>C	ENSP00000515181.1:n.*770G>C
ENST00000703131.1:n.1199G>C
ENST00000703139.1:c.32G>C
ENST00000703140.1:c.5182G>C	ENSP00000515197.1:p.Glu1728Gln
ENST00000703141.1:c.*715G>C	ENSP00000515198.1:n.*715G>C
ENST00000703142.1:c.*2225G>C	ENSP00000515199.1:n.*2225G>C
ENST00000361445.9:c.5395G>C MANE Select	ENSP00000354558.4:p.Glu1799Gln
ENST00000361445.8:c.5395G>C	ENSP00000354558.4:p.Glu1799Gln
ENST00000376838.5:c.10G>C	ENSP00000366034.1:p.Glu4Gln
NM_004958.3:c.5395G>C , LRG_734t1:c.5395G>C	NP_004949.1:p.Glu1799Gln
XM_005263438.1:c.5395G>C	XP_005263495.1:p.Glu1799Gln
XR_244786.1:n.5516G>C
XM_005263438.2:c.5395G>C	XP_005263495.1:p.Glu1799Gln
XM_017000900.1:c.4714G>C	XP_016856389.1:p.Glu1572Gln
XM_017000901.1:c.4147G>C	XP_016856390.1:p.Glu1383Gln
XM_024446187.1:c.5395G>C	XP_024301955.1:p.Glu1799Gln
XR_001737087.1:n.5516G>C
NM_004958.4:c.5395G>C MANE Select	NP_004949.1:p.Glu1799Gln
NM_001386500.1:c.5395G>C	NP_001373429.1:p.Glu1799Gln
NM_001386501.1:c.4147G>C	NP_001373430.1:p.Glu1383Gln