Canonical Allele Identifier: CA2522979788

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11156972_11156973insCT , CM000663.2:g.11156972_11156973insCT	GRCh38
NC_000001.10:g.11217029_11217030insCT , CM000663.1:g.11217029_11217030insCT	GRCh37
NC_000001.9:g.11139616_11139617insCT	NCBI36
NG_033239.1:g.110579_110580insAG , LRG_734:g.110579_110580insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.4469+179_4469+180insAG	ENSP00000515181.1:n.4469+179_4469+180insAG
ENST00000703131.1:n.389+179_389+180insAG
ENST00000703140.1:c.4256+179_4256+180insAG	ENSP00000515197.1:n.4256+179_4256+180insAG
ENST00000703141.1:c.4469+179_4469+180insAG	ENSP00000515198.1:n.4469+179_4469+180insAG
ENST00000703142.1:c.*1299+179_*1299+180insAG	ENSP00000515199.1:n.*1299+179_*1299+180insAG
ENST00000361445.9:c.4469+179_4469+180insAG MANE Select	ENSP00000354558.4:n.4469+179_4469+180insAG
ENST00000361445.8:c.4469+179_4469+180insAG	ENSP00000354558.4:n.4469+179_4469+180insAG
NM_004958.3:c.4469+179_4469+180insAG , LRG_734t1:c.4469+179_4469+180insAG	NP_004949.1:n.4469+179_4469+180insAG
XM_005263438.1:c.4469+179_4469+180insAG	XP_005263495.1:n.4469+179_4469+180insAG
XM_011541166.1:c.4469+179_4469+180insAG	XP_011539468.1:n.4469+179_4469+180insAG
XR_244786.1:n.4590+179_4590+180insAG
XM_005263438.2:c.4469+179_4469+180insAG	XP_005263495.1:n.4469+179_4469+180insAG
XM_011541166.2:c.4469+179_4469+180insAG	XP_011539468.1:n.4469+179_4469+180insAG
XM_017000900.1:c.3788+179_3788+180insAG	XP_016856389.1:n.3788+179_3788+180insAG
XM_017000901.1:c.3221+179_3221+180insAG	XP_016856390.1:n.3221+179_3221+180insAG
XM_024446187.1:c.4469+179_4469+180insAG	XP_024301955.1:n.4469+179_4469+180insAG
XR_001737087.1:n.4590+179_4590+180insAG
NM_004958.4:c.4469+179_4469+180insAG MANE Select	NP_004949.1:n.4469+179_4469+180insAG
NM_001386500.1:c.4469+179_4469+180insAG	NP_001373429.1:n.4469+179_4469+180insAG
NM_001386501.1:c.3221+179_3221+180insAG	NP_001373430.1:n.3221+179_3221+180insAG