Canonical Allele Identifier: CA415916576

Gene: MTOR

Linked Data

• MyVariant Identifiers: chr1:g.11169426A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109369A>G , CM000663.2:g.11109369A>G	GRCh38
NC_000001.10:g.11169426A>G , CM000663.1:g.11169426A>G	GRCh37
NC_000001.9:g.11092013A>G	NCBI36
NG_033239.1:g.158183T>C , LRG_734:g.158183T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2824T>C	ENSP00000515181.1:n.*2824T>C
ENST00000703131.1:n.3367T>C
ENST00000703139.1:c.2237T>C
ENST00000703140.1:c.7236T>C	ENSP00000515197.1:p.Ile2412=
ENST00000703141.1:c.*2966T>C	ENSP00000515198.1:n.*2966T>C
ENST00000703142.1:c.*4279T>C	ENSP00000515199.1:n.*4279T>C
ENST00000361445.9:c.7449T>C MANE Select	ENSP00000354558.4:p.Ile2483=
ENST00000361445.8:c.7449T>C	ENSP00000354558.4:p.Ile2483=
ENST00000376838.5:c.2064T>C	ENSP00000366034.1:p.Ile688=
ENST00000455339.1:c.417T>C	ENSP00000398745.1:p.Ile139=
ENST00000473471.5:n.461T>C
ENST00000490931.1:n.732T>C
NM_004958.3:c.7449T>C , LRG_734t1:c.7449T>C	NP_004949.1:p.Ile2483=
XM_005263438.1:c.7449T>C	XP_005263495.1:p.Ile2483=
XM_005263438.2:c.7449T>C	XP_005263495.1:p.Ile2483=
XM_017000900.1:c.6768T>C	XP_016856389.1:p.Ile2256=
XM_017000901.1:c.6201T>C	XP_016856390.1:p.Ile2067=
XM_024446187.1:c.7449T>C	XP_024301955.1:p.Ile2483=
XR_001737087.1:n.7487T>C
NM_004958.4:c.7449T>C MANE Select	NP_004949.1:p.Ile2483=
NM_001386500.1:c.7449T>C	NP_001373429.1:p.Ile2483=
NM_001386501.1:c.6201T>C	NP_001373430.1:p.Ile2067=