Canonical Allele Identifier: CA2278095665
Community Standard Title: NM_020761.3(RPTOR):c.349-27297G=
Gene: RPTOR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80680544G= , CM000679.2:g.80680544G= GRCh38
NC_000017.10:g.78654344G= , CM000679.1:g.78654344G= GRCh37
NC_000017.9:g.76268939G= NCBI36
NG_013034.1:g.140720G=
NG_013034.2:g.140720G=

Transcript Alleles

HGVS Amino-acid Change
NM_020761.3:c.349-27297G= MANE Select NP_065812.1:n.349-27297G=
ENST00000306801.8:c.349-27297G= MANE Select ENSP00000307272.3:n.349-27297G=
NM_001163034.1:c.349-27297G= NP_001156506.1:n.349-27297G=
NM_001163034.2:c.349-27297G= NP_001156506.1:n.349-27297G=
NM_020761.2:c.349-27297G= NP_065812.1:n.349-27297G=
ENST00000306801.7:c.349-27297G= ENSP00000307272.3:n.349-27297G=
ENST00000544334.6:c.349-27297G= ENSP00000442479.2:n.349-27297G=
ENST00000570891.5:c.349-27297G= ENSP00000460136.1:n.349-27297G=
ENST00000574767.5:c.266-27297G= ENSP00000459701.1:n.266-27297G=
ENST00000577161.5:n.1148-27297G=
ENST00000649732.1:n.1105-27297G=
ENST00000697423.1:c.403-27297G= ENSP00000513305.1:n.403-27297G=