Canonical Allele Identifier: CA15247394
Gene: RHOA HGNC NCBI

Linked Data

dbSNP Id: rs8179164
gnomAD v2: 3-49397284-T-A
gnomAD v3: 3-49359851-T-A
gnomAD v4: 3-49359851-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49359851T>A , CM000665.2:g.49359851T>A GRCh38
NC_000003.11:g.49397284T>A , CM000665.1:g.49397284T>A GRCh37
NC_000003.10:g.49372288T>A NCBI36
NG_012264.1:g.3508A>T
NG_051308.1:g.57247A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000704381.1:c.464+476A>T ENSP00000515884.1:n.464+476A>T
ENST00000418115.6:c.*358A>T MANE Select ENSP00000400175.1:n.*358A>T
ENST00000422781.6:c.*515A>T ENSP00000413587.1:n.*515A>T
ENST00000445425.6:c.*358A>T ENSP00000408402.3:n.*358A>T
ENST00000454011.7:c.*546A>T ENSP00000394483.2:n.*546A>T
ENST00000676712.2:c.*358A>T ENSP00000504603.1:n.*358A>T
ENST00000678200.1:c.*358A>T ENSP00000504180.1:n.*358A>T
ENST00000678921.2:c.*2639A>T ENSP00000503490.1:n.*2639A>T
ENST00000679208.1:c.*358A>T ENSP00000503282.1:n.*358A>T
ENST00000418115.5:c.*358A>T ENSP00000400175.1:n.*358A>T
NM_001313941.1:c.*358A>T NP_001300870.1:n.*358A>T
NM_001313943.1:c.*515A>T NP_001300872.1:n.*515A>T
NM_001313944.1:c.*358A>T NP_001300873.1:n.*358A>T
NM_001313945.1:c.*358A>T NP_001300874.1:n.*358A>T
NM_001313946.1:c.*358A>T NP_001300875.1:n.*358A>T
NM_001313947.1:c.*546A>T NP_001300876.1:n.*546A>T
NM_001664.2:c.*358A>T NP_001655.1:n.*358A>T
NM_001664.3:c.*358A>T NP_001655.1:n.*358A>T
XM_011533695.1:c.*358A>T XP_011531997.1:n.*358A>T
NM_001664.4:c.*358A>T MANE Select NP_001655.1:n.*358A>T
NM_001313941.2:c.*358A>T NP_001300870.1:n.*358A>T
NM_001313943.2:c.*515A>T NP_001300872.1:n.*515A>T
NM_001313944.2:c.*358A>T NP_001300873.1:n.*358A>T
NM_001313945.2:c.*358A>T NP_001300874.1:n.*358A>T
NM_001313946.2:c.*358A>T NP_001300875.1:n.*358A>T
NM_001313947.2:c.*546A>T NP_001300876.1:n.*546A>T