Canonical Allele Identifier: CA1153502573

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11109312G= , CM000663.2:g.11109312G=	GRCh38
NC_000001.10:g.11169369G= , CM000663.1:g.11169369G=	GRCh37
NC_000001.9:g.11091956G=	NCBI36
NG_033239.1:g.158240C= , LRG_734:g.158240C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2881C=	ENSP00000515181.1:n.*2881C=
ENST00000703131.1:n.3424C=
ENST00000703139.1:c.2294C=
ENST00000703140.1:c.7293C=	ENSP00000515197.1:p.Asn2431=
ENST00000703141.1:c.*3023C=	ENSP00000515198.1:n.*3023C=
ENST00000703142.1:c.*4336C=	ENSP00000515199.1:n.*4336C=
ENST00000361445.9:c.7506C= MANE Select	ENSP00000354558.4:p.Asn2502=
ENST00000361445.8:c.7506C=	ENSP00000354558.4:p.Asn2502=
ENST00000376838.5:c.2121C=	ENSP00000366034.1:p.Asn707=
ENST00000455339.1:c.474C=	ENSP00000398745.1:p.Asn158=
ENST00000473471.5:n.518C=
ENST00000490931.1:n.789C=
NM_004958.3:c.7506C= , LRG_734t1:c.7506C=	NP_004949.1:p.Asn2502=
XM_005263438.1:c.7506C=	XP_005263495.1:p.Asn2502=
XM_005263438.2:c.7506C=	XP_005263495.1:p.Asn2502=
XM_017000900.1:c.6825C=	XP_016856389.1:p.Asn2275=
XM_017000901.1:c.6258C=	XP_016856390.1:p.Asn2086=
XM_024446187.1:c.7506C=	XP_024301955.1:p.Asn2502=
XR_001737087.1:n.7544C=
NM_004958.4:c.7506C= MANE Select	NP_004949.1:p.Asn2502=
NM_001386500.1:c.7506C=	NP_001373429.1:p.Asn2502=
NM_001386501.1:c.6258C=	NP_001373430.1:p.Asn2086=