Canonical Allele Identifier: CA521158077

Gene: MTOR

Linked Data

• dbSNP Id: rs1292067053
• gnomAD v2: 1-11217182-CA-C
• MyVariant Identifiers: chr1:g.11217183del (hg19) ; chr1:g.11157126del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11157126del , CM000663.2:g.11157126del	GRCh38
NC_000001.10:g.11217183del , CM000663.1:g.11217183del	GRCh37
NC_000001.9:g.11139770del	NCBI36
NG_033239.1:g.110426del , LRG_734:g.110426del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.4469+26del	ENSP00000515181.1:n.4469+26del
ENST00000703131.1:n.389+26del
ENST00000703140.1:c.4256+26del	ENSP00000515197.1:n.4256+26del
ENST00000703141.1:c.4469+26del	ENSP00000515198.1:n.4469+26del
ENST00000703142.1:c.*1299+26del	ENSP00000515199.1:n.*1299+26del
ENST00000361445.9:c.4469+26del MANE Select	ENSP00000354558.4:n.4469+26del
ENST00000361445.8:c.4469+26del	ENSP00000354558.4:n.4469+26del
NM_004958.3:c.4469+26del , LRG_734t1:c.4469+26del	NP_004949.1:n.4469+26del
XM_005263438.1:c.4469+26del	XP_005263495.1:n.4469+26del
XM_011541166.1:c.4469+26del	XP_011539468.1:n.4469+26del
XR_244786.1:n.4590+26del
XM_005263438.2:c.4469+26del	XP_005263495.1:n.4469+26del
XM_011541166.2:c.4469+26del	XP_011539468.1:n.4469+26del
XM_017000900.1:c.3788+26del	XP_016856389.1:n.3788+26del
XM_017000901.1:c.3221+26del	XP_016856390.1:n.3221+26del
XM_024446187.1:c.4469+26del	XP_024301955.1:n.4469+26del
XR_001737087.1:n.4590+26del
NM_004958.4:c.4469+26del MANE Select	NP_004949.1:n.4469+26del
NM_001386500.1:c.4469+26del	NP_001373429.1:n.4469+26del
NM_001386501.1:c.3221+26del	NP_001373430.1:n.3221+26del