Canonical Allele Identifier: CA2643238895

Gene: MTOR

Linked Data

• gnomAD v4: 1-11109419-CAGGTTCAATGGGTGCCCTGTTTTTCTCAAATATTCACTTTTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109420_11109461del , CM000663.2:g.11109420_11109461del	GRCh38
NC_000001.10:g.11169477_11169518del , CM000663.1:g.11169477_11169518del	GRCh37
NC_000001.9:g.11092064_11092105del	NCBI36
NG_033239.1:g.158091_158132del , LRG_734:g.158091_158132del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2823-91_*2823-50del	ENSP00000515181.1:n.*2823-91_*2823-50del
ENST00000703131.1:n.3366-91_3366-50del
ENST00000703139.1:c.2236-91_2236-50del
ENST00000703140.1:c.7235-91_7235-50del	ENSP00000515197.1:n.7235-91_7235-50del
ENST00000703141.1:c.*2965-91_*2965-50del	ENSP00000515198.1:n.*2965-91_*2965-50del
ENST00000703142.1:c.*4278-91_*4278-50del	ENSP00000515199.1:n.*4278-91_*4278-50del
ENST00000361445.9:c.7448-91_7448-50del MANE Select	ENSP00000354558.4:n.7448-91_7448-50del
ENST00000361445.8:c.7448-91_7448-50del	ENSP00000354558.4:n.7448-91_7448-50del
ENST00000376838.5:c.2063-91_2063-50del	ENSP00000366034.1:n.2063-91_2063-50del
ENST00000455339.1:c.416-91_416-50del	ENSP00000398745.1:n.416-91_416-50del
ENST00000473471.5:n.460-91_460-50del
ENST00000490931.1:n.731-91_731-50del
NM_004958.3:c.7448-91_7448-50del , LRG_734t1:c.7448-91_7448-50del	NP_004949.1:n.7448-91_7448-50del
XM_005263438.1:c.7448-91_7448-50del	XP_005263495.1:n.7448-91_7448-50del
XM_005263438.2:c.7448-91_7448-50del	XP_005263495.1:n.7448-91_7448-50del
XM_017000900.1:c.6767-91_6767-50del	XP_016856389.1:n.6767-91_6767-50del
XM_017000901.1:c.6200-91_6200-50del	XP_016856390.1:n.6200-91_6200-50del
XM_024446187.1:c.7448-91_7448-50del	XP_024301955.1:n.7448-91_7448-50del
XR_001737087.1:n.7486-91_7486-50del
NM_004958.4:c.7448-91_7448-50del MANE Select	NP_004949.1:n.7448-91_7448-50del
NM_001386500.1:c.7448-91_7448-50del	NP_001373429.1:n.7448-91_7448-50del
NM_001386501.1:c.6200-91_6200-50del	NP_001373430.1:n.6200-91_6200-50del