Canonical Allele Identifier: CA1752687373

Gene: RHEB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151490872A= , CM000669.2:g.151490872A=	GRCh38
NC_000007.13:g.151187958A= , CM000669.1:g.151187958A=	GRCh37
NC_000007.12:g.150818891A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262187.10:c.124+71T= MANE Select	ENSP00000262187.5:n.124+71T=
ENST00000262187.9:c.124+71T=	ENSP00000262187.5:n.124+71T=
ENST00000470370.1:c.-192+71T=	ENSP00000417212.1:n.-192+71T=
ENST00000472642.5:c.-192+71T=	ENSP00000420726.1:n.-192+71T=
ENST00000478470.5:c.*72+71T=	ENSP00000417802.1:n.*72+71T=
ENST00000496004.5:c.-192+71T=	ENSP00000418161.1:n.-192+71T=
NM_005614.3:c.124+71T=	NP_005605.1:n.124+71T=
XM_011516457.1:c.91+71T=	XP_011514759.1:n.91+71T=
XM_011516457.2:c.91+71T=	XP_011514759.1:n.91+71T=
XM_024446854.1:c.91+71T=	XP_024302622.1:n.91+71T=
NM_005614.4:c.124+71T= MANE Select	NP_005605.1:n.124+71T=