Canonical Allele Identifier: CA338378702

Gene: MTOR

Linked Data

• dbSNP Id: rs1641738942
• gnomAD v4: 1-11109344-C-A
• MyVariant Identifiers: chr1:g.11169401C>A (hg19) ; chr1:g.11109344C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109344C>A , CM000663.2:g.11109344C>A	GRCh38
NC_000001.10:g.11169401C>A , CM000663.1:g.11169401C>A	GRCh37
NC_000001.9:g.11091988C>A	NCBI36
NG_033239.1:g.158208G>T , LRG_734:g.158208G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2849G>T	ENSP00000515181.1:n.*2849G>T
ENST00000703131.1:n.3392G>T
ENST00000703139.1:c.2262G>T
ENST00000703140.1:c.7261G>T	ENSP00000515197.1:p.Ala2421Ser
ENST00000703141.1:c.*2991G>T	ENSP00000515198.1:n.*2991G>T
ENST00000703142.1:c.*4304G>T	ENSP00000515199.1:n.*4304G>T
ENST00000361445.9:c.7474G>T MANE Select	ENSP00000354558.4:p.Ala2492Ser
ENST00000361445.8:c.7474G>T	ENSP00000354558.4:p.Ala2492Ser
ENST00000376838.5:c.2089G>T	ENSP00000366034.1:p.Ala697Ser
ENST00000455339.1:c.442G>T	ENSP00000398745.1:p.Ala148Ser
ENST00000473471.5:n.486G>T
ENST00000490931.1:n.757G>T
NM_004958.3:c.7474G>T , LRG_734t1:c.7474G>T	NP_004949.1:p.Ala2492Ser
XM_005263438.1:c.7474G>T	XP_005263495.1:p.Ala2492Ser
XM_005263438.2:c.7474G>T	XP_005263495.1:p.Ala2492Ser
XM_017000900.1:c.6793G>T	XP_016856389.1:p.Ala2265Ser
XM_017000901.1:c.6226G>T	XP_016856390.1:p.Ala2076Ser
XM_024446187.1:c.7474G>T	XP_024301955.1:p.Ala2492Ser
XR_001737087.1:n.7512G>T
NM_004958.4:c.7474G>T MANE Select	NP_004949.1:p.Ala2492Ser
NM_001386500.1:c.7474G>T	NP_001373429.1:p.Ala2492Ser
NM_001386501.1:c.6226G>T	NP_001373430.1:p.Ala2076Ser