Canonical Allele Identifier: CA2643238907

Gene: MTOR

Linked Data

• gnomAD v4: 1-11109459-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109459T>C , CM000663.2:g.11109459T>C	GRCh38
NC_000001.10:g.11169516T>C , CM000663.1:g.11169516T>C	GRCh37
NC_000001.9:g.11092103T>C	NCBI36
NG_033239.1:g.158093A>G , LRG_734:g.158093A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2823-89A>G	ENSP00000515181.1:n.*2823-89A>G
ENST00000703131.1:n.3366-89A>G
ENST00000703139.1:c.2236-89A>G
ENST00000703140.1:c.7235-89A>G	ENSP00000515197.1:n.7235-89A>G
ENST00000703141.1:c.*2965-89A>G	ENSP00000515198.1:n.*2965-89A>G
ENST00000703142.1:c.*4278-89A>G	ENSP00000515199.1:n.*4278-89A>G
ENST00000361445.9:c.7448-89A>G MANE Select	ENSP00000354558.4:n.7448-89A>G
ENST00000361445.8:c.7448-89A>G	ENSP00000354558.4:n.7448-89A>G
ENST00000376838.5:c.2063-89A>G	ENSP00000366034.1:n.2063-89A>G
ENST00000455339.1:c.416-89A>G	ENSP00000398745.1:n.416-89A>G
ENST00000473471.5:n.460-89A>G
ENST00000490931.1:n.731-89A>G
NM_004958.3:c.7448-89A>G , LRG_734t1:c.7448-89A>G	NP_004949.1:n.7448-89A>G
XM_005263438.1:c.7448-89A>G	XP_005263495.1:n.7448-89A>G
XM_005263438.2:c.7448-89A>G	XP_005263495.1:n.7448-89A>G
XM_017000900.1:c.6767-89A>G	XP_016856389.1:n.6767-89A>G
XM_017000901.1:c.6200-89A>G	XP_016856390.1:n.6200-89A>G
XM_024446187.1:c.7448-89A>G	XP_024301955.1:n.7448-89A>G
XR_001737087.1:n.7486-89A>G
NM_004958.4:c.7448-89A>G MANE Select	NP_004949.1:n.7448-89A>G
NM_001386500.1:c.7448-89A>G	NP_001373429.1:n.7448-89A>G
NM_001386501.1:c.6200-89A>G	NP_001373430.1:n.6200-89A>G