Canonical Allele Identifier: CA1363448456
Gene: RHOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49359861G= , CM000665.2:g.49359861G= GRCh38
NC_000003.11:g.49397294G= , CM000665.1:g.49397294G= GRCh37
NC_000003.10:g.49372298G= NCBI36
NG_012264.1:g.3498C=
NG_051308.1:g.57237C=

Transcript Alleles

HGVS Amino-acid change
ENST00000704381.1:c.464+466C= ENSP00000515884.1:n.464+466C=
ENST00000418115.6:c.*348C= MANE Select ENSP00000400175.1:n.*348C=
ENST00000422781.6:c.*505C= ENSP00000413587.1:n.*505C=
ENST00000445425.6:c.*348C= ENSP00000408402.3:n.*348C=
ENST00000454011.7:c.*536C= ENSP00000394483.2:n.*536C=
ENST00000676712.2:c.*348C= ENSP00000504603.1:n.*348C=
ENST00000678200.1:c.*348C= ENSP00000504180.1:n.*348C=
ENST00000678921.2:c.*2629C= ENSP00000503490.1:n.*2629C=
ENST00000679208.1:c.*348C= ENSP00000503282.1:n.*348C=
ENST00000418115.5:c.*348C= ENSP00000400175.1:n.*348C=
NM_001313941.1:c.*348C= NP_001300870.1:n.*348C=
NM_001313943.1:c.*505C= NP_001300872.1:n.*505C=
NM_001313944.1:c.*348C= NP_001300873.1:n.*348C=
NM_001313945.1:c.*348C= NP_001300874.1:n.*348C=
NM_001313946.1:c.*348C= NP_001300875.1:n.*348C=
NM_001313947.1:c.*536C= NP_001300876.1:n.*536C=
NM_001664.2:c.*348C= NP_001655.1:n.*348C=
NM_001664.3:c.*348C= NP_001655.1:n.*348C=
XM_011533695.1:c.*348C= XP_011531997.1:n.*348C=
NM_001664.4:c.*348C= MANE Select NP_001655.1:n.*348C=
NM_001313941.2:c.*348C= NP_001300870.1:n.*348C=
NM_001313943.2:c.*505C= NP_001300872.1:n.*505C=
NM_001313944.2:c.*348C= NP_001300873.1:n.*348C=
NM_001313945.2:c.*348C= NP_001300874.1:n.*348C=
NM_001313946.2:c.*348C= NP_001300875.1:n.*348C=
NM_001313947.2:c.*536C= NP_001300876.1:n.*536C=