Canonical Allele Identifier: CA338378530

Gene: MTOR

Linked Data

• MyVariant Identifiers: chr1:g.11169353G>T (hg19) ; chr1:g.11109296G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109296G>T , CM000663.2:g.11109296G>T	GRCh38
NC_000001.10:g.11169353G>T , CM000663.1:g.11169353G>T	GRCh37
NC_000001.9:g.11091940G>T	NCBI36
NG_033239.1:g.158256C>A , LRG_734:g.158256C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2897C>A	ENSP00000515181.1:n.*2897C>A
ENST00000703131.1:n.3440C>A
ENST00000703139.1:c.2310C>A
ENST00000703140.1:c.7309C>A	ENSP00000515197.1:p.Leu2437Ile
ENST00000703141.1:c.*3039C>A	ENSP00000515198.1:n.*3039C>A
ENST00000703142.1:c.*4352C>A	ENSP00000515199.1:n.*4352C>A
ENST00000361445.9:c.7522C>A MANE Select	ENSP00000354558.4:p.Leu2508Ile
ENST00000361445.8:c.7522C>A	ENSP00000354558.4:p.Leu2508Ile
ENST00000376838.5:c.2137C>A	ENSP00000366034.1:p.Leu713Ile
ENST00000473471.5:n.534C>A
ENST00000490931.1:n.805C>A
NM_004958.3:c.7522C>A , LRG_734t1:c.7522C>A	NP_004949.1:p.Leu2508Ile
XM_005263438.1:c.7522C>A	XP_005263495.1:p.Leu2508Ile
XM_005263438.2:c.7522C>A	XP_005263495.1:p.Leu2508Ile
XM_017000900.1:c.6841C>A	XP_016856389.1:p.Leu2281Ile
XM_017000901.1:c.6274C>A	XP_016856390.1:p.Leu2092Ile
XM_024446187.1:c.7522C>A	XP_024301955.1:p.Leu2508Ile
XR_001737087.1:n.7560C>A
NM_004958.4:c.7522C>A MANE Select	NP_004949.1:p.Leu2508Ile
NM_001386500.1:c.7522C>A	NP_001373429.1:p.Leu2508Ile
NM_001386501.1:c.6274C>A	NP_001373430.1:p.Leu2092Ile