Canonical Allele Identifier: CA338378679

Gene: MTOR

Linked Data

• dbSNP Id: rs2100287096
• MyVariant Identifiers: chr1:g.11169394T>C (hg19) ; chr1:g.11109337T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109337T>C , CM000663.2:g.11109337T>C	GRCh38
NC_000001.10:g.11169394T>C , CM000663.1:g.11169394T>C	GRCh37
NC_000001.9:g.11091981T>C	NCBI36
NG_033239.1:g.158215A>G , LRG_734:g.158215A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2856A>G	ENSP00000515181.1:n.*2856A>G
ENST00000703131.1:n.3399A>G
ENST00000703139.1:c.2269A>G
ENST00000703140.1:c.7268A>G	ENSP00000515197.1:p.Asn2423Ser
ENST00000703141.1:c.*2998A>G	ENSP00000515198.1:n.*2998A>G
ENST00000703142.1:c.*4311A>G	ENSP00000515199.1:n.*4311A>G
ENST00000361445.9:c.7481A>G MANE Select	ENSP00000354558.4:p.Asn2494Ser
ENST00000361445.8:c.7481A>G	ENSP00000354558.4:p.Asn2494Ser
ENST00000376838.5:c.2096A>G	ENSP00000366034.1:p.Asn699Ser
ENST00000455339.1:c.449A>G	ENSP00000398745.1:p.Asn150Ser
ENST00000473471.5:n.493A>G
ENST00000490931.1:n.764A>G
NM_004958.3:c.7481A>G , LRG_734t1:c.7481A>G	NP_004949.1:p.Asn2494Ser
XM_005263438.1:c.7481A>G	XP_005263495.1:p.Asn2494Ser
XM_005263438.2:c.7481A>G	XP_005263495.1:p.Asn2494Ser
XM_017000900.1:c.6800A>G	XP_016856389.1:p.Asn2267Ser
XM_017000901.1:c.6233A>G	XP_016856390.1:p.Asn2078Ser
XM_024446187.1:c.7481A>G	XP_024301955.1:p.Asn2494Ser
XR_001737087.1:n.7519A>G
NM_004958.4:c.7481A>G MANE Select	NP_004949.1:p.Asn2494Ser
NM_001386500.1:c.7481A>G	NP_001373429.1:p.Asn2494Ser
NM_001386501.1:c.6233A>G	NP_001373430.1:p.Asn2078Ser