Canonical Allele Identifier: CA521171508

Gene: MTOR

Linked Data

• dbSNP Id: rs1329221615
• gnomAD v2: 1-11171175-T-TG
• gnomAD v3: 1-11111118-T-TG
• gnomAD v4: 1-11111118-T-TG
• MyVariant Identifiers: chr1:g.11171175_11171176insG (hg19) ; chr1:g.11111118_11111119insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11111118_11111119insG , CM000663.2:g.11111118_11111119insG	GRCh38
NC_000001.10:g.11171175_11171176insG , CM000663.1:g.11171175_11171176insG	GRCh37
NC_000001.9:g.11093762_11093763insG	NCBI36
NG_033239.1:g.156433_156434insC , LRG_734:g.156433_156434insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2742-1390_*2742-1389insC	ENSP00000515181.1:n.*2742-1390_*2742-1389insC
ENST00000703131.1:n.3285-1390_3285-1389insC
ENST00000703139.1:c.2155-1390_2155-1389insC
ENST00000703140.1:c.7154-1390_7154-1389insC	ENSP00000515197.1:n.7154-1390_7154-1389insC
ENST00000703141.1:c.*2884-1390_*2884-1389insC	ENSP00000515198.1:n.*2884-1390_*2884-1389insC
ENST00000703142.1:c.*4197-1390_*4197-1389insC	ENSP00000515199.1:n.*4197-1390_*4197-1389insC
ENST00000361445.9:c.7367-1390_7367-1389insC MANE Select	ENSP00000354558.4:n.7367-1390_7367-1389insC
ENST00000361445.8:c.7367-1390_7367-1389insC	ENSP00000354558.4:n.7367-1390_7367-1389insC
ENST00000376838.5:c.1982-1390_1982-1389insC	ENSP00000366034.1:n.1982-1390_1982-1389insC
ENST00000455339.1:c.335-1390_335-1389insC	ENSP00000398745.1:n.335-1390_335-1389insC
ENST00000473471.5:n.379-1390_379-1389insC
ENST00000490931.1:n.649+395_649+396insC
NM_004958.3:c.7367-1390_7367-1389insC , LRG_734t1:c.7367-1390_7367-1389insC	NP_004949.1:n.7367-1390_7367-1389insC
XM_005263438.1:c.7367-1390_7367-1389insC	XP_005263495.1:n.7367-1390_7367-1389insC
XM_005263438.2:c.7367-1390_7367-1389insC	XP_005263495.1:n.7367-1390_7367-1389insC
XM_017000900.1:c.6686-1390_6686-1389insC	XP_016856389.1:n.6686-1390_6686-1389insC
XM_017000901.1:c.6119-1390_6119-1389insC	XP_016856390.1:n.6119-1390_6119-1389insC
XM_024446187.1:c.7367-1390_7367-1389insC	XP_024301955.1:n.7367-1390_7367-1389insC
XR_001737087.1:n.7405-1390_7405-1389insC
NM_004958.4:c.7367-1390_7367-1389insC MANE Select	NP_004949.1:n.7367-1390_7367-1389insC
NM_001386500.1:c.7367-1390_7367-1389insC	NP_001373429.1:n.7367-1390_7367-1389insC
NM_001386501.1:c.6119-1390_6119-1389insC	NP_001373430.1:n.6119-1390_6119-1389insC