Canonical Allele Identifier: CA2685694655

Gene: RHEB

Linked Data

• gnomAD v4: 7-151491058-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151491058G>T , CM000669.2:g.151491058G>T	GRCh38
NC_000007.13:g.151188144G>T , CM000669.1:g.151188144G>T	GRCh37
NC_000007.12:g.150819077G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262187.10:c.53-44C>A MANE Select	ENSP00000262187.5:n.53-44C>A
ENST00000262187.9:c.53-44C>A	ENSP00000262187.5:n.53-44C>A
ENST00000470370.1:c.-263-44C>A	ENSP00000417212.1:n.-263-44C>A
ENST00000472642.5:c.-263-44C>A	ENSP00000420726.1:n.-263-44C>A
ENST00000478470.5:c.*1-44C>A	ENSP00000417802.1:n.*1-44C>A
ENST00000496004.5:c.-263-44C>A	ENSP00000418161.1:n.-263-44C>A
NM_005614.3:c.53-44C>A	NP_005605.1:n.53-44C>A
XM_011516457.1:c.20-44C>A	XP_011514759.1:n.20-44C>A
XM_011516457.2:c.20-44C>A	XP_011514759.1:n.20-44C>A
XM_024446854.1:c.20-44C>A	XP_024302622.1:n.20-44C>A
NM_005614.4:c.53-44C>A MANE Select	NP_005605.1:n.53-44C>A