Canonical Allele Identifier: CA278804
Gene: CDC42 HGNC NCBI

Linked Data

ClinVar Variation Id: 218950
ClinVar RCV Id: RCV000203307 RCV000489915 RCV001266021 RCV001291421
dbSNP Id: rs864309721
MyVariant Identifiers: chr1:g.22412944A>G (hg19) chr1:g.22086451A>G (hg38)
PubMed: PMID:26386261 PMID:26708094
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22086451A>G , CM000663.2:g.22086451A>G GRCh38
NC_000001.10:g.22412944A>G , CM000663.1:g.22412944A>G GRCh37
NC_000001.9:g.22285531A>G NCBI36
NG_047042.1:g.38825A>G
NG_047042.2:g.38743A>G
NG_047042.3:g.65941A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000315554.15:c.191A>G ENSP00000314458.8:p.Tyr64Cys
ENST00000344548.8:c.191A>G ENSP00000341072.3:p.Tyr64Cys
ENST00000411827.2:c.191A>G ENSP00000398327.2:p.Tyr64Cys
ENST00000662562.2:c.191A>G ENSP00000499612.1:p.Tyr64Cys
ENST00000667384.2:c.191A>G ENSP00000499473.1:p.Tyr64Cys
ENST00000695796.1:c.191A>G ENSP00000512176.1:p.Tyr64Cys
ENST00000695797.1:c.191A>G ENSP00000512177.1:p.Tyr64Cys
ENST00000695798.1:c.191A>G ENSP00000512178.1:p.Tyr64Cys
ENST00000695799.1:c.191A>G ENSP00000512179.1:p.Tyr64Cys
ENST00000695800.1:c.191A>G ENSP00000512180.1:p.Tyr64Cys
ENST00000695801.1:c.191A>G ENSP00000512181.1:p.Tyr64Cys
ENST00000695802.1:c.191A>G ENSP00000512182.1:p.Tyr64Cys
ENST00000695855.1:c.191A>G ENSP00000512220.1:p.Tyr64Cys
ENST00000695856.1:c.191A>G ENSP00000512221.1:p.Tyr64Cys
ENST00000695857.1:c.191A>G ENSP00000512222.1:p.Tyr64Cys
ENST00000695858.1:c.191A>G ENSP00000512223.1:p.Tyr64Cys
ENST00000695859.1:c.191A>G ENSP00000512224.1:p.Tyr64Cys
ENST00000695860.1:c.191A>G ENSP00000512225.1:p.Tyr64Cys
ENST00000695861.1:c.*241A>G ENSP00000512226.1:n.*241A>G
ENST00000695862.1:c.118A>G ENSP00000512227.1:p.Met40Val
ENST00000695863.1:c.*241A>G ENSP00000512228.1:n.*241A>G
ENST00000315554.13:c.191A>G ENSP00000314458.8:p.Tyr64Cys
ENST00000648594.1:c.191A>G ENSP00000497733.1:p.Tyr64Cys
ENST00000651171.1:c.191A>G ENSP00000499132.1:p.Tyr64Cys
ENST00000652582.1:c.326A>G ENSP00000498275.1:p.Tyr109Cys
ENST00000656825.1:c.191A>G MANE Select ENSP00000499457.1:p.Tyr64Cys
ENST00000662562.1:c.191A>G ENSP00000499612.1:p.Tyr64Cys
ENST00000667384.1:c.191A>G ENSP00000499473.1:p.Tyr64Cys
ENST00000315554.12:c.191A>G ENSP00000314458.8:p.Tyr64Cys
ENST00000344548.7:c.191A>G ENSP00000341072.3:p.Tyr64Cys
ENST00000400259.5:c.191A>G ENSP00000383118.1:p.Tyr64Cys
ENST00000411827.1:c.191A>G ENSP00000398327.1:p.Tyr64Cys
ENST00000498236.1:n.453A>G
NM_001039802.1:c.191A>G NP_001034891.1:p.Tyr64Cys
NM_001791.3:c.191A>G NP_001782.1:p.Tyr64Cys
NM_044472.2:c.191A>G NP_426359.1:p.Tyr64Cys
NM_001791.4:c.191A>G MANE Select NP_001782.1:p.Tyr64Cys
NM_001039802.2:c.191A>G NP_001034891.1:p.Tyr64Cys
NM_044472.3:c.191A>G NP_426359.1:p.Tyr64Cys
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