Canonical Allele Identifier: CA10937093
Community Standard Title: NM_004958.4(MTOR):c.6663-78C>T
Gene: MTOR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11122204G>A , CM000663.2:g.11122204G>A GRCh38
NC_000001.10:g.11182261G>A , CM000663.1:g.11182261G>A GRCh37
NC_000001.9:g.11104848G>A NCBI36
NG_033239.1:g.145348C>T , LRG_734:g.145348C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004958.4:c.6663-78C>T MANE Select NP_004949.1:n.6663-78C>T
ENST00000361445.9:c.6663-78C>T MANE Select ENSP00000354558.4:n.6663-78C>T
NM_001386500.1:c.6663-78C>T NP_001373429.1:n.6663-78C>T
NM_001386501.1:c.5415-78C>T NP_001373430.1:n.5415-78C>T
NM_004958.3:c.6663-78C>T , LRG_734t1:c.6663-78C>T NP_004949.1:n.6663-78C>T
ENST00000361445.8:c.6663-78C>T ENSP00000354558.4:n.6663-78C>T
ENST00000376838.5:c.1278-78C>T ENSP00000366034.1:n.1278-78C>T
ENST00000703118.1:c.*2038-78C>T ENSP00000515181.1:n.*2038-78C>T
ENST00000703131.1:n.2664-78C>T
ENST00000703139.1:c.1300-78C>T
ENST00000703140.1:c.6450-78C>T ENSP00000515197.1:n.6450-78C>T
ENST00000703141.1:c.*2180-78C>T ENSP00000515198.1:n.*2180-78C>T
ENST00000703142.1:c.*3493-78C>T ENSP00000515199.1:n.*3493-78C>T
XM_005263438.1:c.6663-78C>T XP_005263495.1:n.6663-78C>T
XM_005263438.2:c.6663-78C>T XP_005263495.1:n.6663-78C>T
XM_017000900.1:c.5982-78C>T XP_016856389.1:n.5982-78C>T
XM_017000901.1:c.5415-78C>T XP_016856390.1:n.5415-78C>T
XM_024446187.1:c.6663-78C>T XP_024301955.1:n.6663-78C>T
XR_001737087.1:n.6784-78C>T
XR_244786.1:n.6784-78C>T