Canonical Allele Identifier: CA415916536

Gene: MTOR

Linked Data

• dbSNP Id: rs1057519915
• MyVariant Identifiers: chr1:g.11169375A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109318A>T , CM000663.2:g.11109318A>T	GRCh38
NC_000001.10:g.11169375A>T , CM000663.1:g.11169375A>T	GRCh37
NC_000001.9:g.11091962A>T	NCBI36
NG_033239.1:g.158234T>A , LRG_734:g.158234T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000703118.1:c.*2875T>A	ENSP00000515181.1:n.*2875T>A
ENST00000703131.1:n.3418T>A
ENST00000703139.1:c.2288T>A
ENST00000703140.1:c.7287T>A	ENSP00000515197.1:p.Ile2429=
ENST00000703141.1:c.*3017T>A	ENSP00000515198.1:n.*3017T>A
ENST00000703142.1:c.*4330T>A	ENSP00000515199.1:n.*4330T>A
ENST00000361445.9:c.7500T>A MANE Select	ENSP00000354558.4:p.Ile2500=
ENST00000361445.8:c.7500T>A	ENSP00000354558.4:p.Ile2500=
ENST00000376838.5:c.2115T>A	ENSP00000366034.1:p.Ile705=
ENST00000455339.1:c.468T>A	ENSP00000398745.1:p.Ile156=
ENST00000473471.5:n.512T>A
ENST00000490931.1:n.783T>A
NM_004958.3:c.7500T>A , LRG_734t1:c.7500T>A	NP_004949.1:p.Ile2500=
XM_005263438.1:c.7500T>A	XP_005263495.1:p.Ile2500=
XM_005263438.2:c.7500T>A	XP_005263495.1:p.Ile2500=
XM_017000900.1:c.6819T>A	XP_016856389.1:p.Ile2273=
XM_017000901.1:c.6252T>A	XP_016856390.1:p.Ile2084=
XM_024446187.1:c.7500T>A	XP_024301955.1:p.Ile2500=
XR_001737087.1:n.7538T>A
NM_004958.4:c.7500T>A MANE Select	NP_004949.1:p.Ile2500=
NM_001386500.1:c.7500T>A	NP_001373429.1:p.Ile2500=
NM_001386501.1:c.6252T>A	NP_001373430.1:p.Ile2084=