Canonical Allele Identifier: CA338371596

Gene: MTOR

Linked Data

• dbSNP Id: rs1475390394
• MyVariant Identifiers: chr1:g.11217236A>C (hg19) ; chr1:g.11157179A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11157179A>C , CM000663.2:g.11157179A>C	GRCh38
NC_000001.10:g.11217236A>C , CM000663.1:g.11217236A>C	GRCh37
NC_000001.9:g.11139823A>C	NCBI36
NG_033239.1:g.110373T>G , LRG_734:g.110373T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000703118.1:c.4442T>G	ENSP00000515181.1:p.Met1481Arg
ENST00000703131.1:n.362T>G
ENST00000703140.1:c.4229T>G	ENSP00000515197.1:p.Met1410Arg
ENST00000703141.1:c.4442T>G	ENSP00000515198.1:p.Met1481Arg
ENST00000703142.1:c.*1272T>G	ENSP00000515199.1:n.*1272T>G
ENST00000361445.9:c.4442T>G MANE Select	ENSP00000354558.4:p.Met1481Arg
ENST00000361445.8:c.4442T>G	ENSP00000354558.4:p.Met1481Arg
NM_004958.3:c.4442T>G , LRG_734t1:c.4442T>G	NP_004949.1:p.Met1481Arg
XM_005263438.1:c.4442T>G	XP_005263495.1:p.Met1481Arg
XM_011541166.1:c.4442T>G	XP_011539468.1:p.Met1481Arg
XR_244786.1:n.4563T>G
XM_005263438.2:c.4442T>G	XP_005263495.1:p.Met1481Arg
XM_011541166.2:c.4442T>G	XP_011539468.1:p.Met1481Arg
XM_017000900.1:c.3761T>G	XP_016856389.1:p.Met1254Arg
XM_017000901.1:c.3194T>G	XP_016856390.1:p.Met1065Arg
XM_024446187.1:c.4442T>G	XP_024301955.1:p.Met1481Arg
XR_001737087.1:n.4563T>G
NM_004958.4:c.4442T>G MANE Select	NP_004949.1:p.Met1481Arg
NM_001386500.1:c.4442T>G	NP_001373429.1:p.Met1481Arg
NM_001386501.1:c.3194T>G	NP_001373430.1:p.Met1065Arg