Canonical Allele Identifier: CA338378802

Gene: MTOR

Linked Data

• MyVariant Identifiers: chr1:g.11169427A>T (hg19) ; chr1:g.11109370A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109370A>T , CM000663.2:g.11109370A>T	GRCh38
NC_000001.10:g.11169427A>T , CM000663.1:g.11169427A>T	GRCh37
NC_000001.9:g.11092014A>T	NCBI36
NG_033239.1:g.158182T>A , LRG_734:g.158182T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2823T>A	ENSP00000515181.1:n.*2823T>A
ENST00000703131.1:n.3366T>A
ENST00000703139.1:c.2236T>A
ENST00000703140.1:c.7235T>A	ENSP00000515197.1:p.Ile2412Asn
ENST00000703141.1:c.*2965T>A	ENSP00000515198.1:n.*2965T>A
ENST00000703142.1:c.*4278T>A	ENSP00000515199.1:n.*4278T>A
ENST00000361445.9:c.7448T>A MANE Select	ENSP00000354558.4:p.Ile2483Asn
ENST00000361445.8:c.7448T>A	ENSP00000354558.4:p.Ile2483Asn
ENST00000376838.5:c.2063T>A	ENSP00000366034.1:p.Ile688Asn
ENST00000455339.1:c.416T>A	ENSP00000398745.1:p.Ile139Asn
ENST00000473471.5:n.460T>A
ENST00000490931.1:n.731T>A
NM_004958.3:c.7448T>A , LRG_734t1:c.7448T>A	NP_004949.1:p.Ile2483Asn
XM_005263438.1:c.7448T>A	XP_005263495.1:p.Ile2483Asn
XM_005263438.2:c.7448T>A	XP_005263495.1:p.Ile2483Asn
XM_017000900.1:c.6767T>A	XP_016856389.1:p.Ile2256Asn
XM_017000901.1:c.6200T>A	XP_016856390.1:p.Ile2067Asn
XM_024446187.1:c.7448T>A	XP_024301955.1:p.Ile2483Asn
XR_001737087.1:n.7486T>A
NM_004958.4:c.7448T>A MANE Select	NP_004949.1:p.Ile2483Asn
NM_001386500.1:c.7448T>A	NP_001373429.1:p.Ile2483Asn
NM_001386501.1:c.6200T>A	NP_001373430.1:p.Ile2067Asn