Canonical Allele Identifier: CA1153519794

Gene: MTOR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11117039C= , CM000663.2:g.11117039C=	GRCh38
NC_000001.10:g.11177096C= , CM000663.1:g.11177096C=	GRCh37
NC_000001.9:g.11099683C=	NCBI36
NG_033239.1:g.150513G= , LRG_734:g.150513G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703118.1:c.*2356G=	ENSP00000515181.1:n.*2356G=
ENST00000703131.1:n.2935-1571G=
ENST00000703139.1:c.1769G=
ENST00000703140.1:c.6768G=	ENSP00000515197.1:p.Met2256=
ENST00000703141.1:c.*2498G=	ENSP00000515198.1:n.*2498G=
ENST00000703142.1:c.*3811G=	ENSP00000515199.1:n.*3811G=
ENST00000361445.9:c.6981G= MANE Select	ENSP00000354558.4:p.Met2327=
ENST00000361445.8:c.6981G=	ENSP00000354558.4:p.Met2327=
ENST00000376838.5:c.1596G=	ENSP00000366034.1:p.Met532=
NM_004958.3:c.6981G= , LRG_734t1:c.6981G=	NP_004949.1:p.Met2327=
XM_005263438.1:c.6981G=	XP_005263495.1:p.Met2327=
XR_244786.1:n.7055-1571G=
XM_005263438.2:c.6981G=	XP_005263495.1:p.Met2327=
XM_017000900.1:c.6300G=	XP_016856389.1:p.Met2100=
XM_017000901.1:c.5733G=	XP_016856390.1:p.Met1911=
XM_024446187.1:c.6981G=	XP_024301955.1:p.Met2327=
XR_001737087.1:n.7055-1571G=
NM_004958.4:c.6981G= MANE Select	NP_004949.1:p.Met2327=
NM_001386500.1:c.6981G=	NP_001373429.1:p.Met2327=
NM_001386501.1:c.5733G=	NP_001373430.1:p.Met1911=