Canonical Allele Identifier: CA2557400832

Gene: RHOA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49359798_49359799insAA , CM000665.2:g.49359798_49359799insAA	GRCh38
NC_000003.11:g.49397231_49397232insAA , CM000665.1:g.49397231_49397232insAA	GRCh37
NC_000003.10:g.49372235_49372236insAA	NCBI36
NG_012264.1:g.3561_3562insTT
NG_051308.1:g.57300_57301insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704381.1:c.464+529_464+530insTT	ENSP00000515884.1:n.464+529_464+530insTT
ENST00000418115.6:c.*411_*412insTT MANE Select	ENSP00000400175.1:n.*411_*412insTT
ENST00000422781.6:c.*568_*569insTT	ENSP00000413587.1:n.*568_*569insTT
ENST00000445425.6:c.*411_*412insTT	ENSP00000408402.3:n.*411_*412insTT
ENST00000454011.7:c.*599_*600insTT	ENSP00000394483.2:n.*599_*600insTT
ENST00000676712.2:c.*411_*412insTT	ENSP00000504603.1:n.*411_*412insTT
ENST00000678200.1:c.*411_*412insTT	ENSP00000504180.1:n.*411_*412insTT
ENST00000678921.2:c.*2692_*2693insTT	ENSP00000503490.1:n.*2692_*2693insTT
ENST00000679208.1:c.*411_*412insTT	ENSP00000503282.1:n.*411_*412insTT
ENST00000418115.5:c.*411_*412insTT	ENSP00000400175.1:n.*411_*412insTT
NM_001313941.1:c.*411_*412insTT	NP_001300870.1:n.*411_*412insTT
NM_001313943.1:c.*568_*569insTT	NP_001300872.1:n.*568_*569insTT
NM_001313944.1:c.*411_*412insTT	NP_001300873.1:n.*411_*412insTT
NM_001313945.1:c.*411_*412insTT	NP_001300874.1:n.*411_*412insTT
NM_001313946.1:c.*411_*412insTT	NP_001300875.1:n.*411_*412insTT
NM_001313947.1:c.*599_*600insTT	NP_001300876.1:n.*599_*600insTT
NM_001664.2:c.*411_*412insTT	NP_001655.1:n.*411_*412insTT
NM_001664.3:c.*411_*412insTT	NP_001655.1:n.*411_*412insTT
XM_011533695.1:c.*411_*412insTT	XP_011531997.1:n.*411_*412insTT
NM_001664.4:c.*411_*412insTT MANE Select	NP_001655.1:n.*411_*412insTT
NM_001313941.2:c.*411_*412insTT	NP_001300870.1:n.*411_*412insTT
NM_001313943.2:c.*568_*569insTT	NP_001300872.1:n.*568_*569insTT
NM_001313944.2:c.*411_*412insTT	NP_001300873.1:n.*411_*412insTT
NM_001313945.2:c.*411_*412insTT	NP_001300874.1:n.*411_*412insTT
NM_001313946.2:c.*411_*412insTT	NP_001300875.1:n.*411_*412insTT
NM_001313947.2:c.*599_*600insTT	NP_001300876.1:n.*599_*600insTT