Canonical Allele Identifier: CA338378773

Gene: MTOR

Linked Data

• MyVariant Identifiers: chr1:g.11169420G>T (hg19) ; chr1:g.11109363G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109363G>T , CM000663.2:g.11109363G>T	GRCh38
NC_000001.10:g.11169420G>T , CM000663.1:g.11169420G>T	GRCh37
NC_000001.9:g.11092007G>T	NCBI36
NG_033239.1:g.158189C>A , LRG_734:g.158189C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2830C>A	ENSP00000515181.1:n.*2830C>A
ENST00000703131.1:n.3373C>A
ENST00000703139.1:c.2243C>A
ENST00000703140.1:c.7242C>A	ENSP00000515197.1:p.Asp2414Glu
ENST00000703141.1:c.*2972C>A	ENSP00000515198.1:n.*2972C>A
ENST00000703142.1:c.*4285C>A	ENSP00000515199.1:n.*4285C>A
ENST00000361445.9:c.7455C>A MANE Select	ENSP00000354558.4:p.Asp2485Glu
ENST00000361445.8:c.7455C>A	ENSP00000354558.4:p.Asp2485Glu
ENST00000376838.5:c.2070C>A	ENSP00000366034.1:p.Asp690Glu
ENST00000455339.1:c.423C>A	ENSP00000398745.1:p.Asp141Glu
ENST00000473471.5:n.467C>A
ENST00000490931.1:n.738C>A
NM_004958.3:c.7455C>A , LRG_734t1:c.7455C>A	NP_004949.1:p.Asp2485Glu
XM_005263438.1:c.7455C>A	XP_005263495.1:p.Asp2485Glu
XM_005263438.2:c.7455C>A	XP_005263495.1:p.Asp2485Glu
XM_017000900.1:c.6774C>A	XP_016856389.1:p.Asp2258Glu
XM_017000901.1:c.6207C>A	XP_016856390.1:p.Asp2069Glu
XM_024446187.1:c.7455C>A	XP_024301955.1:p.Asp2485Glu
XR_001737087.1:n.7493C>A
NM_004958.4:c.7455C>A MANE Select	NP_004949.1:p.Asp2485Glu
NM_001386500.1:c.7455C>A	NP_001373429.1:p.Asp2485Glu
NM_001386501.1:c.6207C>A	NP_001373430.1:p.Asp2069Glu