Canonical Allele Identifier: CA338371469

Gene: MTOR

Linked Data

• dbSNP Id: rs2100566828
• gnomAD v4: 1-11157156-C-A
• MyVariant Identifiers: chr1:g.11217213C>A (hg19) ; chr1:g.11157156C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11157156C>A , CM000663.2:g.11157156C>A	GRCh38
NC_000001.10:g.11217213C>A , CM000663.1:g.11217213C>A	GRCh37
NC_000001.9:g.11139800C>A	NCBI36
NG_033239.1:g.110396G>T , LRG_734:g.110396G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.4465G>T	ENSP00000515181.1:p.Glu1489Ter
ENST00000703131.1:n.385G>T
ENST00000703140.1:c.4252G>T	ENSP00000515197.1:p.Glu1418Ter
ENST00000703141.1:c.4465G>T	ENSP00000515198.1:p.Glu1489Ter
ENST00000703142.1:c.*1295G>T	ENSP00000515199.1:n.*1295G>T
ENST00000361445.9:c.4465G>T MANE Select	ENSP00000354558.4:p.Glu1489Ter
ENST00000361445.8:c.4465G>T	ENSP00000354558.4:p.Glu1489Ter
NM_004958.3:c.4465G>T , LRG_734t1:c.4465G>T	NP_004949.1:p.Glu1489Ter
XM_005263438.1:c.4465G>T	XP_005263495.1:p.Glu1489Ter
XM_011541166.1:c.4465G>T	XP_011539468.1:p.Glu1489Ter
XR_244786.1:n.4586G>T
XM_005263438.2:c.4465G>T	XP_005263495.1:p.Glu1489Ter
XM_011541166.2:c.4465G>T	XP_011539468.1:p.Glu1489Ter
XM_017000900.1:c.3784G>T	XP_016856389.1:p.Glu1262Ter
XM_017000901.1:c.3217G>T	XP_016856390.1:p.Glu1073Ter
XM_024446187.1:c.4465G>T	XP_024301955.1:p.Glu1489Ter
XR_001737087.1:n.4586G>T
NM_004958.4:c.4465G>T MANE Select	NP_004949.1:p.Glu1489Ter
NM_001386500.1:c.4465G>T	NP_001373429.1:p.Glu1489Ter
NM_001386501.1:c.3217G>T	NP_001373430.1:p.Glu1073Ter