Canonical Allele Identifier: CA338909618

Gene: CDC42

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.22091452G>A , CM000663.2:g.22091452G>A	GRCh38
NC_000001.10:g.22417945G>A , CM000663.1:g.22417945G>A	GRCh37
NC_000001.9:g.22290532G>A	NCBI36
NG_047042.1:g.43826G>A
NG_047042.2:g.43744G>A
NG_047042.3:g.70942G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001791.4:c.511G>A MANE Select	NP_001782.1:p.Glu171Lys
ENST00000656825.1:c.511G>A MANE Select	ENSP00000499457.1:p.Glu171Lys
NM_001039802.1:c.511G>A	NP_001034891.1:p.Glu171Lys
NM_001039802.2:c.511G>A	NP_001034891.1:p.Glu171Lys
NM_001791.3:c.511G>A	NP_001782.1:p.Glu171Lys
ENST00000344548.7:c.511G>A	ENSP00000341072.3:p.Glu171Lys
ENST00000344548.8:c.511G>A	ENSP00000341072.3:p.Glu171Lys
ENST00000400259.5:c.511G>A	ENSP00000383118.1:p.Glu171Lys
ENST00000411827.2:c.511G>A	ENSP00000398327.2:p.Glu171Lys
ENST00000648594.1:c.511G>A	ENSP00000497733.1:p.Glu171Lys
ENST00000662562.1:c.511G>A	ENSP00000499612.1:p.Glu171Lys
ENST00000662562.2:c.511G>A	ENSP00000499612.1:p.Glu171Lys
ENST00000667384.2:c.*4571G>A	ENSP00000499473.1:n.*4571G>A
ENST00000695796.1:c.511G>A	ENSP00000512176.1:p.Glu171Lys
ENST00000695797.1:c.511G>A	ENSP00000512177.1:p.Glu171Lys
ENST00000695798.1:c.511G>A	ENSP00000512178.1:p.Glu171Lys
ENST00000695799.1:c.511G>A	ENSP00000512179.1:p.Glu171Lys
ENST00000695800.1:c.511G>A	ENSP00000512180.1:p.Glu171Lys
ENST00000695801.1:c.*15G>A	ENSP00000512181.1:n.*15G>A
ENST00000695802.1:c.511G>A	ENSP00000512182.1:p.Glu171Lys
ENST00000695855.1:c.*1420G>A	ENSP00000512220.1:n.*1420G>A
ENST00000695856.1:c.511G>A	ENSP00000512221.1:p.Glu171Lys
ENST00000695857.1:c.*1420G>A	ENSP00000512222.1:n.*1420G>A
ENST00000695858.1:c.*15G>A	ENSP00000512223.1:n.*15G>A
ENST00000695859.1:c.*4571G>A	ENSP00000512224.1:n.*4571G>A
ENST00000695860.1:c.*1420G>A	ENSP00000512225.1:n.*1420G>A
ENST00000695861.1:c.*2046G>A	ENSP00000512226.1:n.*2046G>A
ENST00000695862.1:c.*300G>A	ENSP00000512227.1:n.*300G>A