Canonical Allele Identifier: CA204641

Gene: CDC42

Linked Data

• ClinVar Variation Id: 208668
• ClinVar RCV Id: RCV000190678 ; RCV000601199 ; RCV001291422
• dbSNP Id: rs797044870
• gnomAD v4: 1-22086456-A-G
• MyVariant Identifiers: chr1:g.22412949A>G (hg19) ; chr1:g.22086456A>G (hg38)
• PubMed: PMID:7473653 ; PMID:8103286 ; PMID:10898977 ; PMID:11025683 ; PMID:11149925 ; PMID:11864373 ; PMID:12195014 ; PMID:12478284 ; PMID:12687501 ; PMID:12915473 ; PMID:14561717 ; PMID:15269155 ; PMID:15884002 ; PMID:16949823 ; PMID:17050694 ; PMID:17540168 ; PMID:17918734 ; PMID:17970806 ; PMID:18245432 ; PMID:18511961 ; PMID:19092927 ; PMID:19700661 ; PMID:20633244 ; PMID:20878268 ; PMID:21423166 ; PMID:21515363 ; PMID:22266952 ; PMID:23382385 ; PMID:24059268 ; PMID:26386261 ; PMID:26785492 ; PMID:29394990

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22086456A>G , CM000663.2:g.22086456A>G	GRCh38
NC_000001.10:g.22412949A>G , CM000663.1:g.22412949A>G	GRCh37
NC_000001.9:g.22285536A>G	NCBI36
NG_047042.1:g.38830A>G
NG_047042.2:g.38748A>G
NG_047042.3:g.65946A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315554.15:c.196A>G	ENSP00000314458.8:p.Arg66Gly
ENST00000344548.8:c.196A>G	ENSP00000341072.3:p.Arg66Gly
ENST00000411827.2:c.196A>G	ENSP00000398327.2:p.Arg66Gly
ENST00000662562.2:c.196A>G	ENSP00000499612.1:p.Arg66Gly
ENST00000667384.2:c.196A>G	ENSP00000499473.1:p.Arg66Gly
ENST00000695796.1:c.196A>G	ENSP00000512176.1:p.Arg66Gly
ENST00000695797.1:c.196A>G	ENSP00000512177.1:p.Arg66Gly
ENST00000695798.1:c.196A>G	ENSP00000512178.1:p.Arg66Gly
ENST00000695799.1:c.196A>G	ENSP00000512179.1:p.Arg66Gly
ENST00000695800.1:c.196A>G	ENSP00000512180.1:p.Arg66Gly
ENST00000695801.1:c.196A>G	ENSP00000512181.1:p.Arg66Gly
ENST00000695802.1:c.196A>G	ENSP00000512182.1:p.Arg66Gly
ENST00000695855.1:c.196A>G	ENSP00000512220.1:p.Arg66Gly
ENST00000695856.1:c.196A>G	ENSP00000512221.1:p.Arg66Gly
ENST00000695857.1:c.196A>G	ENSP00000512222.1:p.Arg66Gly
ENST00000695858.1:c.196A>G	ENSP00000512223.1:p.Arg66Gly
ENST00000695859.1:c.196A>G	ENSP00000512224.1:p.Arg66Gly
ENST00000695860.1:c.196A>G	ENSP00000512225.1:p.Arg66Gly
ENST00000695861.1:c.*246A>G	ENSP00000512226.1:n.*246A>G
ENST00000695862.1:c.123A>G	ENSP00000512227.1:p.Thr41=
ENST00000695863.1:c.*246A>G	ENSP00000512228.1:n.*246A>G
ENST00000315554.13:c.196A>G	ENSP00000314458.8:p.Arg66Gly
ENST00000648594.1:c.196A>G	ENSP00000497733.1:p.Arg66Gly
ENST00000651171.1:c.196A>G	ENSP00000499132.1:p.Arg66Gly
ENST00000652582.1:c.331A>G	ENSP00000498275.1:p.Arg111Gly
ENST00000656825.1:c.196A>G MANE Select	ENSP00000499457.1:p.Arg66Gly
ENST00000662562.1:c.196A>G	ENSP00000499612.1:p.Arg66Gly
ENST00000667384.1:c.196A>G	ENSP00000499473.1:p.Arg66Gly
ENST00000315554.12:c.196A>G	ENSP00000314458.8:p.Arg66Gly
ENST00000344548.7:c.196A>G	ENSP00000341072.3:p.Arg66Gly
ENST00000400259.5:c.196A>G	ENSP00000383118.1:p.Arg66Gly
ENST00000411827.1:c.196A>G	ENSP00000398327.1:p.Arg66Gly
ENST00000498236.1:n.458A>G
NM_001039802.1:c.196A>G	NP_001034891.1:p.Arg66Gly
NM_001791.3:c.196A>G	NP_001782.1:p.Arg66Gly
NM_044472.2:c.196A>G	NP_426359.1:p.Arg66Gly
NM_001791.4:c.196A>G MANE Select	NP_001782.1:p.Arg66Gly
NM_001039802.2:c.196A>G	NP_001034891.1:p.Arg66Gly
NM_044472.3:c.196A>G	NP_426359.1:p.Arg66Gly