Canonical Allele Identifier: CA1752687496

Gene: RHEB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151491007G= , CM000669.2:g.151491007G=	GRCh38
NC_000007.13:g.151188093G= , CM000669.1:g.151188093G=	GRCh37
NC_000007.12:g.150819026G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262187.10:c.60C= MANE Select	ENSP00000262187.5:p.Ser20=
ENST00000262187.9:c.60C=	ENSP00000262187.5:p.Ser20=
ENST00000470370.1:c.-256C=	ENSP00000417212.1:n.-256C=
ENST00000472642.5:c.-256C=	ENSP00000420726.1:n.-256C=
ENST00000478470.5:c.*8C=	ENSP00000417802.1:n.*8C=
ENST00000496004.5:c.-256C=	ENSP00000418161.1:n.-256C=
NM_005614.3:c.60C=	NP_005605.1:p.Ser20=
XM_011516457.1:c.27C=	XP_011514759.1:p.Ser9=
XM_011516457.2:c.27C=	XP_011514759.1:p.Ser9=
XM_024446854.1:c.27C=	XP_024302622.1:p.Ser9=
NM_005614.4:c.60C= MANE Select	NP_005605.1:p.Ser20=