Canonical Allele Identifier: CA338378543

Gene: MTOR

Linked Data

• MyVariant Identifiers: chr1:g.11169358T>C (hg19) ; chr1:g.11109301T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109301T>C , CM000663.2:g.11109301T>C	GRCh38
NC_000001.10:g.11169358T>C , CM000663.1:g.11169358T>C	GRCh37
NC_000001.9:g.11091945T>C	NCBI36
NG_033239.1:g.158251A>G , LRG_734:g.158251A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2892A>G	ENSP00000515181.1:n.*2892A>G
ENST00000703131.1:n.3435A>G
ENST00000703139.1:c.2305A>G
ENST00000703140.1:c.7304A>G	ENSP00000515197.1:p.Asp2435Gly
ENST00000703141.1:c.*3034A>G	ENSP00000515198.1:n.*3034A>G
ENST00000703142.1:c.*4347A>G	ENSP00000515199.1:n.*4347A>G
ENST00000361445.9:c.7517A>G MANE Select	ENSP00000354558.4:p.Asp2506Gly
ENST00000361445.8:c.7517A>G	ENSP00000354558.4:p.Asp2506Gly
ENST00000376838.5:c.2132A>G	ENSP00000366034.1:p.Asp711Gly
ENST00000473471.5:n.529A>G
ENST00000490931.1:n.800A>G
NM_004958.3:c.7517A>G , LRG_734t1:c.7517A>G	NP_004949.1:p.Asp2506Gly
XM_005263438.1:c.7517A>G	XP_005263495.1:p.Asp2506Gly
XM_005263438.2:c.7517A>G	XP_005263495.1:p.Asp2506Gly
XM_017000900.1:c.6836A>G	XP_016856389.1:p.Asp2279Gly
XM_017000901.1:c.6269A>G	XP_016856390.1:p.Asp2090Gly
XM_024446187.1:c.7517A>G	XP_024301955.1:p.Asp2506Gly
XR_001737087.1:n.7555A>G
NM_004958.4:c.7517A>G MANE Select	NP_004949.1:p.Asp2506Gly
NM_001386500.1:c.7517A>G	NP_001373429.1:p.Asp2506Gly
NM_001386501.1:c.6269A>G	NP_001373430.1:p.Asp2090Gly