Canonical Allele Identifier: CA16042336
Gene: CDC42 HGNC NCBI

Linked Data

ClinVar Variation Id: 372848
ClinVar RCV Id: RCV000414468
dbSNP Id: rs1057518022
MyVariant Identifiers: chr1:g.22408233G>A (hg19) chr1:g.22081740G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22081740G>A , CM000663.2:g.22081740G>A GRCh38
NC_000001.10:g.22408233G>A , CM000663.1:g.22408233G>A GRCh37
NC_000001.9:g.22280820G>A NCBI36
NG_047042.1:g.34114G>A
NG_047042.2:g.34032G>A
NG_047042.3:g.61230G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000315554.15:c.124G>A ENSP00000314458.8:p.Val42Ile
ENST00000344548.8:c.124G>A ENSP00000341072.3:p.Val42Ile
ENST00000411827.2:c.124G>A ENSP00000398327.2:p.Val42Ile
ENST00000662562.2:c.124G>A ENSP00000499612.1:p.Val42Ile
ENST00000667384.2:c.124G>A ENSP00000499473.1:p.Val42Ile
ENST00000695796.1:c.124G>A ENSP00000512176.1:p.Val42Ile
ENST00000695797.1:c.124G>A ENSP00000512177.1:p.Val42Ile
ENST00000695798.1:c.124G>A ENSP00000512178.1:p.Val42Ile
ENST00000695799.1:c.124G>A ENSP00000512179.1:p.Val42Ile
ENST00000695800.1:c.124G>A ENSP00000512180.1:p.Val42Ile
ENST00000695801.1:c.124G>A ENSP00000512181.1:p.Val42Ile
ENST00000695802.1:c.124G>A ENSP00000512182.1:p.Val42Ile
ENST00000695855.1:c.124G>A ENSP00000512220.1:p.Val42Ile
ENST00000695856.1:c.124G>A ENSP00000512221.1:p.Val42Ile
ENST00000695857.1:c.124G>A ENSP00000512222.1:p.Val42Ile
ENST00000695858.1:c.124G>A ENSP00000512223.1:p.Val42Ile
ENST00000695859.1:c.124G>A ENSP00000512224.1:p.Val42Ile
ENST00000695860.1:c.124G>A ENSP00000512225.1:p.Val42Ile
ENST00000695861.1:c.*174G>A ENSP00000512226.1:n.*174G>A
ENST00000695862.1:c.105+3157G>A ENSP00000512227.1:n.105+3157G>A
ENST00000695863.1:c.*174G>A ENSP00000512228.1:n.*174G>A
ENST00000315554.13:c.124G>A ENSP00000314458.8:p.Val42Ile
ENST00000648594.1:c.124G>A ENSP00000497733.1:p.Val42Ile
ENST00000651171.1:c.124G>A ENSP00000499132.1:p.Val42Ile
ENST00000652582.1:c.259G>A ENSP00000498275.1:p.Val87Ile
ENST00000656825.1:c.124G>A MANE Select ENSP00000499457.1:p.Val42Ile
ENST00000662562.1:c.124G>A ENSP00000499612.1:p.Val42Ile
ENST00000667384.1:c.124G>A ENSP00000499473.1:p.Val42Ile
ENST00000315554.12:c.124G>A ENSP00000314458.8:p.Val42Ile
ENST00000344548.7:c.124G>A ENSP00000341072.3:p.Val42Ile
ENST00000400259.5:c.124G>A ENSP00000383118.1:p.Val42Ile
ENST00000411827.1:c.124G>A ENSP00000398327.1:p.Val42Ile
ENST00000498236.1:n.386G>A
NM_001039802.1:c.124G>A NP_001034891.1:p.Val42Ile
NM_001791.3:c.124G>A NP_001782.1:p.Val42Ile
NM_044472.2:c.124G>A NP_426359.1:p.Val42Ile
NM_001791.4:c.124G>A MANE Select NP_001782.1:p.Val42Ile
NM_001039802.2:c.124G>A NP_001034891.1:p.Val42Ile
NM_044472.3:c.124G>A NP_426359.1:p.Val42Ile
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