Canonical Allele Identifier: CA16602953
Gene: RHOA HGNC NCBI

Linked Data

ClinVar Variation Id: 376524
dbSNP Id: rs1057519954

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49375465T>A , CM000665.2:g.49375465T>A GRCh38
NC_000003.11:g.49412898T>A , CM000665.1:g.49412898T>A GRCh37
NC_000003.10:g.49387902T>A NCBI36
NG_051308.1:g.41633A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000704381.1:c.125A>T ENSP00000515884.1:p.Tyr42Phe
ENST00000418115.6:c.125A>T MANE Select ENSP00000400175.1:p.Tyr42Phe
ENST00000422781.6:c.125A>T ENSP00000413587.1:p.Tyr42Phe
ENST00000445425.6:c.125A>T ENSP00000408402.3:p.Tyr42Phe
ENST00000454011.7:c.125A>T ENSP00000394483.2:p.Tyr42Phe
ENST00000676712.2:c.125A>T ENSP00000504603.1:p.Tyr42Phe
ENST00000677684.1:c.125A>T ENSP00000504494.1:p.Tyr42Phe
ENST00000678200.1:c.125A>T ENSP00000504180.1:p.Tyr42Phe
ENST00000678921.2:c.125A>T ENSP00000503490.1:p.Tyr42Phe
ENST00000679208.1:c.125A>T ENSP00000503282.1:p.Tyr42Phe
ENST00000418115.5:c.125A>T ENSP00000400175.1:p.Tyr42Phe
ENST00000422781.5:c.125A>T ENSP00000413587.1:p.Tyr42Phe
ENST00000431929.2:n.405A>T
ENST00000445425.4:c.125A>T ENSP00000408402.1:p.Tyr42Phe
ENST00000454011.6:c.125A>T ENSP00000394483.2:p.Tyr42Phe
NM_001313941.1:c.125A>T NP_001300870.1:p.Tyr42Phe
NM_001313943.1:c.125A>T NP_001300872.1:p.Tyr42Phe
NM_001313944.1:c.125A>T NP_001300873.1:p.Tyr42Phe
NM_001313945.1:c.-119A>T NP_001300874.1:n.-119A>T
NM_001313946.1:c.125A>T NP_001300875.1:p.Tyr42Phe
NM_001313947.1:c.125A>T NP_001300876.1:p.Tyr42Phe
NM_001664.2:c.125A>T NP_001655.1:p.Tyr42Phe
NM_001664.3:c.125A>T NP_001655.1:p.Tyr42Phe
XM_011533695.1:c.125A>T XP_011531997.1:p.Tyr42Phe
NM_001664.4:c.125A>T MANE Select NP_001655.1:p.Tyr42Phe
NM_001313941.2:c.125A>T NP_001300870.1:p.Tyr42Phe
NM_001313943.2:c.125A>T NP_001300872.1:p.Tyr42Phe
NM_001313944.2:c.125A>T NP_001300873.1:p.Tyr42Phe
NM_001313945.2:c.-119A>T NP_001300874.1:n.-119A>T
NM_001313946.2:c.125A>T NP_001300875.1:p.Tyr42Phe
NM_001313947.2:c.125A>T NP_001300876.1:p.Tyr42Phe