Canonical Allele Identifier: CA433652837

Gene: RHOA

Linked Data

• dbSNP Id: rs1057519952
• MyVariant Identifiers: chr3:g.49413010G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49375577G>T , CM000665.2:g.49375577G>T	GRCh38
NC_000003.11:g.49413010G>T , CM000665.1:g.49413010G>T	GRCh37
NC_000003.10:g.49388014G>T	NCBI36
NG_051308.1:g.41521C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000704381.1:c.13C>A	ENSP00000515884.1:p.Arg5=
ENST00000418115.6:c.13C>A MANE Select	ENSP00000400175.1:p.Arg5=
ENST00000422781.6:c.13C>A	ENSP00000413587.1:p.Arg5=
ENST00000445425.6:c.13C>A	ENSP00000408402.3:p.Arg5=
ENST00000454011.7:c.13C>A	ENSP00000394483.2:p.Arg5=
ENST00000676712.2:c.13C>A	ENSP00000504603.1:p.Arg5=
ENST00000677684.1:c.13C>A	ENSP00000504494.1:p.Arg5=
ENST00000678200.1:c.13C>A	ENSP00000504180.1:p.Arg5=
ENST00000678921.2:c.13C>A	ENSP00000503490.1:p.Arg5=
ENST00000679208.1:c.13C>A	ENSP00000503282.1:p.Arg5=
ENST00000418115.5:c.13C>A	ENSP00000400175.1:p.Arg5=
ENST00000422781.5:c.13C>A	ENSP00000413587.1:p.Arg5=
ENST00000431929.2:n.293C>A
ENST00000445425.4:c.13C>A	ENSP00000408402.1:p.Arg5=
ENST00000454011.6:c.13C>A	ENSP00000394483.2:p.Arg5=
NM_001313941.1:c.13C>A	NP_001300870.1:p.Arg5=
NM_001313943.1:c.13C>A	NP_001300872.1:p.Arg5=
NM_001313944.1:c.13C>A	NP_001300873.1:p.Arg5=
NM_001313945.1:c.-147-84C>A	NP_001300874.1:n.-147-84C>A
NM_001313946.1:c.13C>A	NP_001300875.1:p.Arg5=
NM_001313947.1:c.13C>A	NP_001300876.1:p.Arg5=
NM_001664.2:c.13C>A	NP_001655.1:p.Arg5=
NM_001664.3:c.13C>A	NP_001655.1:p.Arg5=
XM_011533695.1:c.13C>A	XP_011531997.1:p.Arg5=
NM_001664.4:c.13C>A MANE Select	NP_001655.1:p.Arg5=
NM_001313941.2:c.13C>A	NP_001300870.1:p.Arg5=
NM_001313943.2:c.13C>A	NP_001300872.1:p.Arg5=
NM_001313944.2:c.13C>A	NP_001300873.1:p.Arg5=
NM_001313945.2:c.-147-84C>A	NP_001300874.1:n.-147-84C>A
NM_001313946.2:c.13C>A	NP_001300875.1:p.Arg5=
NM_001313947.2:c.13C>A	NP_001300876.1:p.Arg5=