Canonical Allele Identifier: CA885449263

Gene: MTOR

Linked Data

• dbSNP Id: rs1371007136
• MyVariant Identifiers: chr1:g.11171230T>A (hg19) ; chr1:g.11111173T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11111173T>A , CM000663.2:g.11111173T>A	GRCh38
NC_000001.10:g.11171230T>A , CM000663.1:g.11171230T>A	GRCh37
NC_000001.9:g.11093817T>A	NCBI36
NG_033239.1:g.156379A>T , LRG_734:g.156379A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2742-1444A>T	ENSP00000515181.1:n.*2742-1444A>T
ENST00000703131.1:n.3285-1444A>T
ENST00000703139.1:c.2155-1444A>T
ENST00000703140.1:c.7154-1444A>T	ENSP00000515197.1:n.7154-1444A>T
ENST00000703141.1:c.*2884-1444A>T	ENSP00000515198.1:n.*2884-1444A>T
ENST00000703142.1:c.*4197-1444A>T	ENSP00000515199.1:n.*4197-1444A>T
ENST00000361445.9:c.7367-1444A>T MANE Select	ENSP00000354558.4:n.7367-1444A>T
ENST00000361445.8:c.7367-1444A>T	ENSP00000354558.4:n.7367-1444A>T
ENST00000376838.5:c.1982-1444A>T	ENSP00000366034.1:n.1982-1444A>T
ENST00000455339.1:c.335-1444A>T	ENSP00000398745.1:n.335-1444A>T
ENST00000473471.5:n.379-1444A>T
ENST00000490931.1:n.649+341A>T
NM_004958.3:c.7367-1444A>T , LRG_734t1:c.7367-1444A>T	NP_004949.1:n.7367-1444A>T
XM_005263438.1:c.7367-1444A>T	XP_005263495.1:n.7367-1444A>T
XM_005263438.2:c.7367-1444A>T	XP_005263495.1:n.7367-1444A>T
XM_017000900.1:c.6686-1444A>T	XP_016856389.1:n.6686-1444A>T
XM_017000901.1:c.6119-1444A>T	XP_016856390.1:n.6119-1444A>T
XM_024446187.1:c.7367-1444A>T	XP_024301955.1:n.7367-1444A>T
XR_001737087.1:n.7405-1444A>T
NM_004958.4:c.7367-1444A>T MANE Select	NP_004949.1:n.7367-1444A>T
NM_001386500.1:c.7367-1444A>T	NP_001373429.1:n.7367-1444A>T
NM_001386501.1:c.6119-1444A>T	NP_001373430.1:n.6119-1444A>T