Canonical Allele Identifier: CA1139772673
Community Standard Title: NM_004958.4(MTOR):c.*829A=
Gene: MTOR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11106656T= , CM000663.2:g.11106656T= GRCh38
NC_000001.10:g.11166713T= , CM000663.1:g.11166713T= GRCh37
NC_000001.9:g.11089300T= NCBI36
NG_033239.1:g.160896A= , LRG_734:g.160896A=

Transcript Alleles

HGVS Amino-acid Change
NM_004958.4:c.*829A= MANE Select NP_004949.1:n.*829A=
ENST00000361445.9:c.*829A= MANE Select ENSP00000354558.4:n.*829A=
NM_001386500.1:c.*829A= NP_001373429.1:n.*829A=
NM_001386501.1:c.*829A= NP_001373430.1:n.*829A=
NM_004958.3:c.*829A= , LRG_734t1:c.*829A= NP_004949.1:n.*829A=
ENST00000361445.8:c.*829A= ENSP00000354558.4:n.*829A=
ENST00000376838.5:c.*829A= ENSP00000366034.1:n.*829A=
ENST00000703118.1:c.*3854A= ENSP00000515181.1:n.*3854A=
ENST00000703139.1:c.3267A=
ENST00000703140.1:c.*829A= ENSP00000515197.1:n.*829A=
ENST00000703141.1:c.*3996A= ENSP00000515198.1:n.*3996A=
ENST00000703142.1:c.*5309A= ENSP00000515199.1:n.*5309A=
XM_005263438.1:c.*829A= XP_005263495.1:n.*829A=
XM_005263438.2:c.*829A= XP_005263495.1:n.*829A=
XM_017000900.1:c.*829A= XP_016856389.1:n.*829A=
XM_017000901.1:c.*829A= XP_016856390.1:n.*829A=
XM_024446187.1:c.*829A= XP_024301955.1:n.*829A=
XR_001737087.1:n.8517A=