Canonical Allele Identifier: CA1363448384
Gene: RHOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49359716C= , CM000665.2:g.49359716C= GRCh38
NC_000003.11:g.49397149C= , CM000665.1:g.49397149C= GRCh37
NC_000003.10:g.49372153C= NCBI36
NG_012264.1:g.3643G=
NG_051308.1:g.57382G=

Transcript Alleles

HGVS Amino-acid change
ENST00000704381.1:c.464+611G= ENSP00000515884.1:n.464+611G=
ENST00000418115.6:c.*493G= MANE Select ENSP00000400175.1:n.*493G=
ENST00000422781.6:c.*650G= ENSP00000413587.1:n.*650G=
ENST00000445425.6:c.*493G= ENSP00000408402.3:n.*493G=
ENST00000454011.7:c.*681G= ENSP00000394483.2:n.*681G=
ENST00000676712.2:c.*493G= ENSP00000504603.1:n.*493G=
ENST00000678200.1:c.*493G= ENSP00000504180.1:n.*493G=
ENST00000678921.2:c.*2774G= ENSP00000503490.1:n.*2774G=
ENST00000679208.1:c.*493G= ENSP00000503282.1:n.*493G=
ENST00000418115.5:c.*493G= ENSP00000400175.1:n.*493G=
NM_001313941.1:c.*493G= NP_001300870.1:n.*493G=
NM_001313943.1:c.*650G= NP_001300872.1:n.*650G=
NM_001313944.1:c.*493G= NP_001300873.1:n.*493G=
NM_001313945.1:c.*493G= NP_001300874.1:n.*493G=
NM_001313946.1:c.*493G= NP_001300875.1:n.*493G=
NM_001313947.1:c.*681G= NP_001300876.1:n.*681G=
NM_001664.2:c.*493G= NP_001655.1:n.*493G=
NM_001664.3:c.*493G= NP_001655.1:n.*493G=
XM_011533695.1:c.*493G= XP_011531997.1:n.*493G=
NM_001664.4:c.*493G= MANE Select NP_001655.1:n.*493G=
NM_001313941.2:c.*493G= NP_001300870.1:n.*493G=
NM_001313943.2:c.*650G= NP_001300872.1:n.*650G=
NM_001313944.2:c.*493G= NP_001300873.1:n.*493G=
NM_001313945.2:c.*493G= NP_001300874.1:n.*493G=
NM_001313946.2:c.*493G= NP_001300875.1:n.*493G=
NM_001313947.2:c.*681G= NP_001300876.1:n.*681G=