Canonical Allele Identifier: CA14495625
Gene: RPTOR HGNC NCBI

Linked Data

dbSNP Id: rs7503807

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80617311A>C , CM000679.2:g.80617311A>C GRCh38
NC_000017.10:g.78591111A>C , CM000679.1:g.78591111A>C GRCh37
NC_000017.9:g.76205706A>C NCBI36
NG_013034.1:g.77487A>C
NG_013034.2:g.77487A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697423.1:c.217-8380A>C ENSP00000513305.1:n.217-8380A>C
ENST00000306801.8:c.163-8380A>C MANE Select ENSP00000307272.3:n.163-8380A>C
ENST00000649732.1:n.919-8380A>C
ENST00000306801.7:c.163-8380A>C ENSP00000307272.3:n.163-8380A>C
ENST00000544334.6:c.163-8380A>C ENSP00000442479.2:n.163-8380A>C
ENST00000570891.5:c.163-8380A>C ENSP00000460136.1:n.163-8380A>C
ENST00000574767.5:c.163-8380A>C ENSP00000459701.1:n.163-8380A>C
ENST00000577161.5:n.962-8380A>C
NM_001163034.1:c.163-8380A>C NP_001156506.1:n.163-8380A>C
NM_020761.2:c.163-8380A>C NP_065812.1:n.163-8380A>C
NM_020761.3:c.163-8380A>C MANE Select NP_065812.1:n.163-8380A>C
NM_001163034.2:c.163-8380A>C NP_001156506.1:n.163-8380A>C