Canonical Allele Identifier: CA645654020

Gene: MTOR

Linked Data

• COSMIC: COSN5730630 ; COSN5730631

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109386G>A , CM000663.2:g.11109386G>A	GRCh38
NC_000001.10:g.11169443G>A , CM000663.1:g.11169443G>A	GRCh37
NC_000001.9:g.11092030G>A	NCBI36
NG_033239.1:g.158166C>T , LRG_734:g.158166C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2823-16C>T	ENSP00000515181.1:n.*2823-16C>T
ENST00000703131.1:n.3366-16C>T
ENST00000703139.1:c.2236-16C>T
ENST00000703140.1:c.7235-16C>T	ENSP00000515197.1:n.7235-16C>T
ENST00000703141.1:c.*2965-16C>T	ENSP00000515198.1:n.*2965-16C>T
ENST00000703142.1:c.*4278-16C>T	ENSP00000515199.1:n.*4278-16C>T
ENST00000361445.9:c.7448-16C>T MANE Select	ENSP00000354558.4:n.7448-16C>T
ENST00000361445.8:c.7448-16C>T	ENSP00000354558.4:n.7448-16C>T
ENST00000376838.5:c.2063-16C>T	ENSP00000366034.1:n.2063-16C>T
ENST00000455339.1:c.416-16C>T	ENSP00000398745.1:n.416-16C>T
ENST00000473471.5:n.460-16C>T
ENST00000490931.1:n.731-16C>T
NM_004958.3:c.7448-16C>T , LRG_734t1:c.7448-16C>T	NP_004949.1:n.7448-16C>T
XM_005263438.1:c.7448-16C>T	XP_005263495.1:n.7448-16C>T
XM_005263438.2:c.7448-16C>T	XP_005263495.1:n.7448-16C>T
XM_017000900.1:c.6767-16C>T	XP_016856389.1:n.6767-16C>T
XM_017000901.1:c.6200-16C>T	XP_016856390.1:n.6200-16C>T
XM_024446187.1:c.7448-16C>T	XP_024301955.1:n.7448-16C>T
XR_001737087.1:n.7486-16C>T
NM_004958.4:c.7448-16C>T MANE Select	NP_004949.1:n.7448-16C>T
NM_001386500.1:c.7448-16C>T	NP_001373429.1:n.7448-16C>T
NM_001386501.1:c.6200-16C>T	NP_001373430.1:n.6200-16C>T