Canonical Allele Identifier: CA2695291243

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11126986C>T , CM000663.2:g.11126986C>T	GRCh38
NC_000001.10:g.11187043C>T , CM000663.1:g.11187043C>T	GRCh37
NC_000001.9:g.11109630C>T	NCBI36
NG_033239.1:g.140566G>A , LRG_734:g.140566G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004958.4:c.6351+24G>A MANE Select	NP_004949.1:n.6351+24G>A
ENST00000361445.9:c.6351+24G>A MANE Select	ENSP00000354558.4:n.6351+24G>A
NM_001386500.1:c.6351+24G>A	NP_001373429.1:n.6351+24G>A
NM_001386501.1:c.5103+24G>A	NP_001373430.1:n.5103+24G>A
NM_004958.3:c.6351+24G>A , LRG_734t1:c.6351+24G>A	NP_004949.1:n.6351+24G>A
ENST00000361445.8:c.6351+24G>A	ENSP00000354558.4:n.6351+24G>A
ENST00000376838.5:c.966+24G>A	ENSP00000366034.1:n.966+24G>A
ENST00000703118.1:c.*1726+24G>A	ENSP00000515181.1:n.*1726+24G>A
ENST00000703131.1:n.2352+24G>A
ENST00000703139.1:c.988+24G>A
ENST00000703140.1:c.6138+24G>A	ENSP00000515197.1:n.6138+24G>A
ENST00000703141.1:c.*1868+24G>A	ENSP00000515198.1:n.*1868+24G>A
ENST00000703142.1:c.*3181+24G>A	ENSP00000515199.1:n.*3181+24G>A
XM_005263438.1:c.6351+24G>A	XP_005263495.1:n.6351+24G>A
XM_005263438.2:c.6351+24G>A	XP_005263495.1:n.6351+24G>A
XM_017000900.1:c.5670+24G>A	XP_016856389.1:n.5670+24G>A
XM_017000901.1:c.5103+24G>A	XP_016856390.1:n.5103+24G>A
XM_024446187.1:c.6351+24G>A	XP_024301955.1:n.6351+24G>A
XR_001737087.1:n.6472+24G>A
XR_244786.1:n.6472+24G>A