Canonical Allele Identifier: CA1363448378

Gene: RHOA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49359707A= , CM000665.2:g.49359707A=	GRCh38
NC_000003.11:g.49397140A= , CM000665.1:g.49397140A=	GRCh37
NC_000003.10:g.49372144A=	NCBI36
NG_012264.1:g.3652T=
NG_051308.1:g.57391T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704381.1:c.464+620T=	ENSP00000515884.1:n.464+620T=
ENST00000418115.6:c.*502T= MANE Select	ENSP00000400175.1:n.*502T=
ENST00000422781.6:c.*659T=	ENSP00000413587.1:n.*659T=
ENST00000445425.6:c.*502T=	ENSP00000408402.3:n.*502T=
ENST00000454011.7:c.*690T=	ENSP00000394483.2:n.*690T=
ENST00000676712.2:c.*502T=	ENSP00000504603.1:n.*502T=
ENST00000678200.1:c.*502T=	ENSP00000504180.1:n.*502T=
ENST00000678921.2:c.*2783T=	ENSP00000503490.1:n.*2783T=
ENST00000679208.1:c.*502T=	ENSP00000503282.1:n.*502T=
ENST00000418115.5:c.*502T=	ENSP00000400175.1:n.*502T=
NM_001313941.1:c.*502T=	NP_001300870.1:n.*502T=
NM_001313943.1:c.*659T=	NP_001300872.1:n.*659T=
NM_001313944.1:c.*502T=	NP_001300873.1:n.*502T=
NM_001313945.1:c.*502T=	NP_001300874.1:n.*502T=
NM_001313946.1:c.*502T=	NP_001300875.1:n.*502T=
NM_001313947.1:c.*690T=	NP_001300876.1:n.*690T=
NM_001664.2:c.*502T=	NP_001655.1:n.*502T=
NM_001664.3:c.*502T=	NP_001655.1:n.*502T=
XM_011533695.1:c.*502T=	XP_011531997.1:n.*502T=
NM_001664.4:c.*502T= MANE Select	NP_001655.1:n.*502T=
NM_001313941.2:c.*502T=	NP_001300870.1:n.*502T=
NM_001313943.2:c.*659T=	NP_001300872.1:n.*659T=
NM_001313944.2:c.*502T=	NP_001300873.1:n.*502T=
NM_001313945.2:c.*502T=	NP_001300874.1:n.*502T=
NM_001313946.2:c.*502T=	NP_001300875.1:n.*502T=
NM_001313947.2:c.*690T=	NP_001300876.1:n.*690T=