Canonical Allele Identifier: CA15891337

Gene: RPTOR

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80650141G>A , CM000679.2:g.80650141G>A	GRCh38
NC_000017.10:g.78623941G>A , CM000679.1:g.78623941G>A	GRCh37
NC_000017.9:g.76238536G>A	NCBI36
NG_013034.1:g.110317G>A
NG_013034.2:g.110317G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697423.1:c.402+6331G>A	ENSP00000513305.1:n.402+6331G>A
ENST00000306801.8:c.348+6331G>A MANE Select	ENSP00000307272.3:n.348+6331G>A
ENST00000649732.1:n.1104+6331G>A
ENST00000306801.7:c.348+6331G>A	ENSP00000307272.3:n.348+6331G>A
ENST00000544334.6:c.348+6331G>A	ENSP00000442479.2:n.348+6331G>A
ENST00000570891.5:c.348+6331G>A	ENSP00000460136.1:n.348+6331G>A
ENST00000574767.5:c.265+24348G>A	ENSP00000459701.1:n.265+24348G>A
ENST00000577161.5:n.1147+6331G>A
NM_001163034.1:c.348+6331G>A	NP_001156506.1:n.348+6331G>A
NM_020761.2:c.348+6331G>A	NP_065812.1:n.348+6331G>A
NM_020761.3:c.348+6331G>A MANE Select	NP_065812.1:n.348+6331G>A
NM_001163034.2:c.348+6331G>A	NP_001156506.1:n.348+6331G>A