Canonical Allele Identifier: CA458661010

Gene: RHEB

Linked Data

• MyVariant Identifiers: chr7:g.151188072A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151490986A>G , CM000669.2:g.151490986A>G	GRCh38
NC_000007.13:g.151188072A>G , CM000669.1:g.151188072A>G	GRCh37
NC_000007.12:g.150819005A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262187.10:c.81T>C MANE Select	ENSP00000262187.5:p.Val27=
ENST00000262187.9:c.81T>C	ENSP00000262187.5:p.Val27=
ENST00000470370.1:c.-235T>C	ENSP00000417212.1:n.-235T>C
ENST00000472642.5:c.-235T>C	ENSP00000420726.1:n.-235T>C
ENST00000478470.5:c.*29T>C	ENSP00000417802.1:n.*29T>C
ENST00000496004.5:c.-235T>C	ENSP00000418161.1:n.-235T>C
NM_005614.3:c.81T>C	NP_005605.1:p.Val27=
XM_011516457.1:c.48T>C	XP_011514759.1:p.Val16=
XM_011516457.2:c.48T>C	XP_011514759.1:p.Val16=
XM_024446854.1:c.48T>C	XP_024302622.1:p.Val16=
NM_005614.4:c.81T>C MANE Select	NP_005605.1:p.Val27=