Canonical Allele Identifier: CA352786720

Gene: RHOA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49368494G>A , CM000665.2:g.49368494G>A	GRCh38
NC_000003.11:g.49405927G>A , CM000665.1:g.49405927G>A	GRCh37
NC_000003.10:g.49380931G>A	NCBI36
NG_051308.1:g.48604C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001664.4:c.211C>T MANE Select	NP_001655.1:p.Pro71Ser
ENST00000418115.6:c.211C>T MANE Select	ENSP00000400175.1:p.Pro71Ser
NM_001313941.1:c.211C>T	NP_001300870.1:p.Pro71Ser
NM_001313941.2:c.211C>T	NP_001300870.1:p.Pro71Ser
NM_001313943.1:c.211C>T	NP_001300872.1:p.Pro71Ser
NM_001313943.2:c.211C>T	NP_001300872.1:p.Pro71Ser
NM_001313944.1:c.151C>T	NP_001300873.1:p.Pro51Ser
NM_001313944.2:c.151C>T	NP_001300873.1:p.Pro51Ser
NM_001313945.1:c.-33C>T	NP_001300874.1:n.-33C>T
NM_001313945.2:c.-33C>T	NP_001300874.1:n.-33C>T
NM_001313946.1:c.156+6940C>T	NP_001300875.1:n.156+6940C>T
NM_001313946.2:c.156+6940C>T	NP_001300875.1:n.156+6940C>T
NM_001313947.1:c.157-5868C>T	NP_001300876.1:n.157-5868C>T
NM_001313947.2:c.157-5868C>T	NP_001300876.1:n.157-5868C>T
NM_001664.2:c.211C>T	NP_001655.1:p.Pro71Ser
NM_001664.3:c.211C>T	NP_001655.1:p.Pro71Ser
ENST00000418115.5:c.211C>T	ENSP00000400175.1:p.Pro71Ser
ENST00000422781.5:c.211C>T	ENSP00000413587.1:p.Pro71Ser
ENST00000422781.6:c.211C>T	ENSP00000413587.1:p.Pro71Ser
ENST00000445425.4:c.211C>T	ENSP00000408402.1:p.Pro71Ser
ENST00000445425.6:c.211C>T	ENSP00000408402.3:p.Pro71Ser
ENST00000454011.6:c.157-5868C>T	ENSP00000394483.2:n.157-5868C>T
ENST00000454011.7:c.157-5868C>T	ENSP00000394483.2:n.157-5868C>T
ENST00000676712.2:c.156+6940C>T	ENSP00000504603.1:n.156+6940C>T
ENST00000677684.1:c.*11C>T	ENSP00000504494.1:n.*11C>T
ENST00000678200.1:c.211C>T	ENSP00000504180.1:p.Pro71Ser
ENST00000678921.2:c.211C>T	ENSP00000503490.1:p.Pro71Ser
ENST00000679208.1:c.211C>T	ENSP00000503282.1:p.Pro71Ser
ENST00000704381.1:c.211C>T	ENSP00000515884.1:p.Pro71Ser
XM_011533695.1:c.211C>T	XP_011531997.1:p.Pro71Ser