Canonical Allele Identifier: CA1363448375
Gene: RHOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49359701A= , CM000665.2:g.49359701A= GRCh38
NC_000003.11:g.49397134A= , CM000665.1:g.49397134A= GRCh37
NC_000003.10:g.49372138A= NCBI36
NG_012264.1:g.3658T=
NG_051308.1:g.57397T=

Transcript Alleles

HGVS Amino-acid change
ENST00000704381.1:c.464+626T= ENSP00000515884.1:n.464+626T=
ENST00000418115.6:c.*508T= MANE Select ENSP00000400175.1:n.*508T=
ENST00000422781.6:c.*665T= ENSP00000413587.1:n.*665T=
ENST00000445425.6:c.*508T= ENSP00000408402.3:n.*508T=
ENST00000454011.7:c.*696T= ENSP00000394483.2:n.*696T=
ENST00000676712.2:c.*508T= ENSP00000504603.1:n.*508T=
ENST00000678200.1:c.*508T= ENSP00000504180.1:n.*508T=
ENST00000678921.2:c.*2789T= ENSP00000503490.1:n.*2789T=
ENST00000679208.1:c.*508T= ENSP00000503282.1:n.*508T=
ENST00000418115.5:c.*508T= ENSP00000400175.1:n.*508T=
NM_001313941.1:c.*508T= NP_001300870.1:n.*508T=
NM_001313943.1:c.*665T= NP_001300872.1:n.*665T=
NM_001313944.1:c.*508T= NP_001300873.1:n.*508T=
NM_001313945.1:c.*508T= NP_001300874.1:n.*508T=
NM_001313946.1:c.*508T= NP_001300875.1:n.*508T=
NM_001313947.1:c.*696T= NP_001300876.1:n.*696T=
NM_001664.2:c.*508T= NP_001655.1:n.*508T=
NM_001664.3:c.*508T= NP_001655.1:n.*508T=
XM_011533695.1:c.*508T= XP_011531997.1:n.*508T=
NM_001664.4:c.*508T= MANE Select NP_001655.1:n.*508T=
NM_001313941.2:c.*508T= NP_001300870.1:n.*508T=
NM_001313943.2:c.*665T= NP_001300872.1:n.*665T=
NM_001313944.2:c.*508T= NP_001300873.1:n.*508T=
NM_001313945.2:c.*508T= NP_001300874.1:n.*508T=
NM_001313946.2:c.*508T= NP_001300875.1:n.*508T=
NM_001313947.2:c.*696T= NP_001300876.1:n.*696T=