Canonical Allele Identifier: CA352786737

Gene: RHOA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49368497T>C , CM000665.2:g.49368497T>C	GRCh38
NC_000003.11:g.49405930T>C , CM000665.1:g.49405930T>C	GRCh37
NC_000003.10:g.49380934T>C	NCBI36
NG_051308.1:g.48601A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001664.4:c.208A>G MANE Select	NP_001655.1:p.Arg70Gly
ENST00000418115.6:c.208A>G MANE Select	ENSP00000400175.1:p.Arg70Gly
NM_001313941.1:c.208A>G	NP_001300870.1:p.Arg70Gly
NM_001313941.2:c.208A>G	NP_001300870.1:p.Arg70Gly
NM_001313943.1:c.208A>G	NP_001300872.1:p.Arg70Gly
NM_001313943.2:c.208A>G	NP_001300872.1:p.Arg70Gly
NM_001313944.1:c.148A>G	NP_001300873.1:p.Arg50Gly
NM_001313944.2:c.148A>G	NP_001300873.1:p.Arg50Gly
NM_001313945.1:c.-36A>G	NP_001300874.1:n.-36A>G
NM_001313945.2:c.-36A>G	NP_001300874.1:n.-36A>G
NM_001313946.1:c.156+6937A>G	NP_001300875.1:n.156+6937A>G
NM_001313946.2:c.156+6937A>G	NP_001300875.1:n.156+6937A>G
NM_001313947.1:c.157-5871A>G	NP_001300876.1:n.157-5871A>G
NM_001313947.2:c.157-5871A>G	NP_001300876.1:n.157-5871A>G
NM_001664.2:c.208A>G	NP_001655.1:p.Arg70Gly
NM_001664.3:c.208A>G	NP_001655.1:p.Arg70Gly
ENST00000418115.5:c.208A>G	ENSP00000400175.1:p.Arg70Gly
ENST00000422781.5:c.208A>G	ENSP00000413587.1:p.Arg70Gly
ENST00000422781.6:c.208A>G	ENSP00000413587.1:p.Arg70Gly
ENST00000445425.4:c.208A>G	ENSP00000408402.1:p.Arg70Gly
ENST00000445425.6:c.208A>G	ENSP00000408402.3:p.Arg70Gly
ENST00000454011.6:c.157-5871A>G	ENSP00000394483.2:n.157-5871A>G
ENST00000454011.7:c.157-5871A>G	ENSP00000394483.2:n.157-5871A>G
ENST00000676712.2:c.156+6937A>G	ENSP00000504603.1:n.156+6937A>G
ENST00000677684.1:c.*8A>G	ENSP00000504494.1:n.*8A>G
ENST00000678200.1:c.208A>G	ENSP00000504180.1:p.Arg70Gly
ENST00000678921.2:c.208A>G	ENSP00000503490.1:p.Arg70Gly
ENST00000679208.1:c.208A>G	ENSP00000503282.1:p.Arg70Gly
ENST00000704381.1:c.208A>G	ENSP00000515884.1:p.Arg70Gly
XM_011533695.1:c.208A>G	XP_011531997.1:p.Arg70Gly