Canonical Allele Identifier: CA2665723614

Gene: RHOA

Linked Data

• gnomAD v4: 3-49359703-TGTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49359704_49359706del , CM000665.2:g.49359704_49359706del	GRCh38
NC_000003.11:g.49397137_49397139del , CM000665.1:g.49397137_49397139del	GRCh37
NC_000003.10:g.49372141_49372143del	NCBI36
NG_012264.1:g.3653_3655del
NG_051308.1:g.57392_57394del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704381.1:c.464+621_464+623del	ENSP00000515884.1:n.464+621_464+623del
ENST00000418115.6:c.*503_*505del MANE Select	ENSP00000400175.1:n.*503_*505del
ENST00000422781.6:c.*660_*662del	ENSP00000413587.1:n.*660_*662del
ENST00000445425.6:c.*503_*505del	ENSP00000408402.3:n.*503_*505del
ENST00000454011.7:c.*691_*693del	ENSP00000394483.2:n.*691_*693del
ENST00000676712.2:c.*503_*505del	ENSP00000504603.1:n.*503_*505del
ENST00000678200.1:c.*503_*505del	ENSP00000504180.1:n.*503_*505del
ENST00000678921.2:c.*2784_*2786del	ENSP00000503490.1:n.*2784_*2786del
ENST00000679208.1:c.*503_*505del	ENSP00000503282.1:n.*503_*505del
ENST00000418115.5:c.*503_*505del	ENSP00000400175.1:n.*503_*505del
NM_001313941.1:c.*503_*505del	NP_001300870.1:n.*503_*505del
NM_001313943.1:c.*660_*662del	NP_001300872.1:n.*660_*662del
NM_001313944.1:c.*503_*505del	NP_001300873.1:n.*503_*505del
NM_001313945.1:c.*503_*505del	NP_001300874.1:n.*503_*505del
NM_001313946.1:c.*503_*505del	NP_001300875.1:n.*503_*505del
NM_001313947.1:c.*691_*693del	NP_001300876.1:n.*691_*693del
NM_001664.2:c.*503_*505del	NP_001655.1:n.*503_*505del
NM_001664.3:c.*503_*505del	NP_001655.1:n.*503_*505del
XM_011533695.1:c.*503_*505del	XP_011531997.1:n.*503_*505del
NM_001664.4:c.*503_*505del MANE Select	NP_001655.1:n.*503_*505del
NM_001313941.2:c.*503_*505del	NP_001300870.1:n.*503_*505del
NM_001313943.2:c.*660_*662del	NP_001300872.1:n.*660_*662del
NM_001313944.2:c.*503_*505del	NP_001300873.1:n.*503_*505del
NM_001313945.2:c.*503_*505del	NP_001300874.1:n.*503_*505del
NM_001313946.2:c.*503_*505del	NP_001300875.1:n.*503_*505del
NM_001313947.2:c.*691_*693del	NP_001300876.1:n.*691_*693del