Canonical Allele Identifier: CA338906652

Gene: CDC42

Linked Data

• ClinVar Variation Id: 450370
• ClinVar RCV Id: RCV000519757 ; RCV001332038 ; RCV001291423
• dbSNP Id: rs1553196096
• MyVariant Identifiers: chr1:g.22412956G>A (hg19) ; chr1:g.22086463G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22086463G>A , CM000663.2:g.22086463G>A	GRCh38
NC_000001.10:g.22412956G>A , CM000663.1:g.22412956G>A	GRCh37
NC_000001.9:g.22285543G>A	NCBI36
NG_047042.1:g.38837G>A
NG_047042.2:g.38755G>A
NG_047042.3:g.65953G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315554.15:c.203G>A	ENSP00000314458.8:p.Arg68Gln
ENST00000344548.8:c.203G>A	ENSP00000341072.3:p.Arg68Gln
ENST00000411827.2:c.203G>A	ENSP00000398327.2:p.Arg68Gln
ENST00000662562.2:c.203G>A	ENSP00000499612.1:p.Arg68Gln
ENST00000667384.2:c.203G>A	ENSP00000499473.1:p.Arg68Gln
ENST00000695796.1:c.203G>A	ENSP00000512176.1:p.Arg68Gln
ENST00000695797.1:c.203G>A	ENSP00000512177.1:p.Arg68Gln
ENST00000695798.1:c.203G>A	ENSP00000512178.1:p.Arg68Gln
ENST00000695799.1:c.203G>A	ENSP00000512179.1:p.Arg68Gln
ENST00000695800.1:c.203G>A	ENSP00000512180.1:p.Arg68Gln
ENST00000695801.1:c.203G>A	ENSP00000512181.1:p.Arg68Gln
ENST00000695802.1:c.203G>A	ENSP00000512182.1:p.Arg68Gln
ENST00000695855.1:c.203G>A	ENSP00000512220.1:p.Arg68Gln
ENST00000695856.1:c.203G>A	ENSP00000512221.1:p.Arg68Gln
ENST00000695857.1:c.203G>A	ENSP00000512222.1:p.Arg68Gln
ENST00000695858.1:c.203G>A	ENSP00000512223.1:p.Arg68Gln
ENST00000695859.1:c.203G>A	ENSP00000512224.1:p.Arg68Gln
ENST00000695860.1:c.203G>A	ENSP00000512225.1:p.Arg68Gln
ENST00000695861.1:c.*253G>A	ENSP00000512226.1:n.*253G>A
ENST00000695862.1:c.130G>A	ENSP00000512227.1:p.Asp44Asn
ENST00000695863.1:c.*253G>A	ENSP00000512228.1:n.*253G>A
ENST00000315554.13:c.203G>A	ENSP00000314458.8:p.Arg68Gln
ENST00000648594.1:c.203G>A	ENSP00000497733.1:p.Arg68Gln
ENST00000651171.1:c.203G>A	ENSP00000499132.1:p.Arg68Gln
ENST00000652582.1:c.338G>A	ENSP00000498275.1:p.Arg113Gln
ENST00000656825.1:c.203G>A MANE Select	ENSP00000499457.1:p.Arg68Gln
ENST00000662562.1:c.203G>A	ENSP00000499612.1:p.Arg68Gln
ENST00000667384.1:c.203G>A	ENSP00000499473.1:p.Arg68Gln
ENST00000315554.12:c.203G>A	ENSP00000314458.8:p.Arg68Gln
ENST00000344548.7:c.203G>A	ENSP00000341072.3:p.Arg68Gln
ENST00000400259.5:c.203G>A	ENSP00000383118.1:p.Arg68Gln
ENST00000411827.1:c.203G>A	ENSP00000398327.1:p.Arg68Gln
ENST00000498236.1:n.465G>A
NM_001039802.1:c.203G>A	NP_001034891.1:p.Arg68Gln
NM_001791.3:c.203G>A	NP_001782.1:p.Arg68Gln
NM_044472.2:c.203G>A	NP_426359.1:p.Arg68Gln
NM_001791.4:c.203G>A MANE Select	NP_001782.1:p.Arg68Gln
NM_001039802.2:c.203G>A	NP_001034891.1:p.Arg68Gln
NM_044472.3:c.203G>A	NP_426359.1:p.Arg68Gln