Canonical Allele Identifier: CA1153506426

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11110982_11110983delinsAG , CM000663.2:g.11110982_11110983delinsAG	GRCh38
NC_000001.10:g.11171039_11171040delinsAG , CM000663.1:g.11171039_11171040delinsAG	GRCh37
NC_000001.9:g.11093626_11093627delinsAG	NCBI36
NG_033239.1:g.156569_156570delinsCT , LRG_734:g.156569_156570delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2742-1254_*2742-1253delinsCT	ENSP00000515181.1:n.*2742-1254_*2742-1253delinsCT
ENST00000703131.1:n.3285-1254_3285-1253delinsCT
ENST00000703139.1:c.2155-1254_2155-1253delinsCT
ENST00000703140.1:c.7154-1254_7154-1253delinsCT	ENSP00000515197.1:n.7154-1254_7154-1253delinsCT
ENST00000703141.1:c.*2884-1254_*2884-1253delinsCT	ENSP00000515198.1:n.*2884-1254_*2884-1253delinsCT
ENST00000703142.1:c.*4197-1254_*4197-1253delinsCT	ENSP00000515199.1:n.*4197-1254_*4197-1253delinsCT
ENST00000361445.9:c.7367-1254_7367-1253delinsCT MANE Select	ENSP00000354558.4:n.7367-1254_7367-1253delinsCT
ENST00000361445.8:c.7367-1254_7367-1253delinsCT	ENSP00000354558.4:n.7367-1254_7367-1253delinsCT
ENST00000376838.5:c.1982-1254_1982-1253delinsCT	ENSP00000366034.1:n.1982-1254_1982-1253delinsCT
ENST00000455339.1:c.335-1254_335-1253delinsCT	ENSP00000398745.1:n.335-1254_335-1253delinsCT
ENST00000473471.5:n.379-1254_379-1253delinsCT
ENST00000490931.1:n.649+531_649+532delinsCT
NM_004958.3:c.7367-1254_7367-1253delinsCT , LRG_734t1:c.7367-1254_7367-1253delinsCT	NP_004949.1:n.7367-1254_7367-1253delinsCT
XM_005263438.1:c.7367-1254_7367-1253delinsCT	XP_005263495.1:n.7367-1254_7367-1253delinsCT
XM_005263438.2:c.7367-1254_7367-1253delinsCT	XP_005263495.1:n.7367-1254_7367-1253delinsCT
XM_017000900.1:c.6686-1254_6686-1253delinsCT	XP_016856389.1:n.6686-1254_6686-1253delinsCT
XM_017000901.1:c.6119-1254_6119-1253delinsCT	XP_016856390.1:n.6119-1254_6119-1253delinsCT
XM_024446187.1:c.7367-1254_7367-1253delinsCT	XP_024301955.1:n.7367-1254_7367-1253delinsCT
XR_001737087.1:n.7405-1254_7405-1253delinsCT
NM_004958.4:c.7367-1254_7367-1253delinsCT MANE Select	NP_004949.1:n.7367-1254_7367-1253delinsCT
NM_001386500.1:c.7367-1254_7367-1253delinsCT	NP_001373429.1:n.7367-1254_7367-1253delinsCT
NM_001386501.1:c.6119-1254_6119-1253delinsCT	NP_001373430.1:n.6119-1254_6119-1253delinsCT