Canonical Allele Identifier: CA1582690914

Gene: CDC42SE2

Linked Data

• dbSNP Id: rs1750074922

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.131373755A>G , CM000667.2:g.131373755A>G	GRCh38
NC_000005.9:g.130709448A>G , CM000667.1:g.130709448A>G	GRCh37
NC_000005.8:g.130737347A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505065.2:c.55-11788A>G MANE Select	ENSP00000427421.1:n.55-11788A>G
ENST00000360515.7:c.55-11788A>G	ENSP00000353706.3:n.55-11788A>G
ENST00000395246.5:c.55-11788A>G	ENSP00000378667.1:n.55-11788A>G
ENST00000503291.5:c.-27-11788A>G	ENSP00000426779.1:n.-27-11788A>G
ENST00000505065.1:c.55-11788A>G	ENSP00000427421.1:n.55-11788A>G
NM_001038702.1:c.55-11788A>G	NP_001033791.1:n.55-11788A>G
NM_020240.2:c.55-11788A>G	NP_064625.1:n.55-11788A>G
XM_017009648.2:c.55-11788A>G	XP_016865137.1:n.55-11788A>G
XM_017009649.2:c.55-11788A>G	XP_016865138.1:n.55-11788A>G
NM_001038702.2:c.55-11788A>G	NP_001033791.1:n.55-11788A>G
NM_001375633.1:c.55-11788A>G	NP_001362562.1:n.55-11788A>G
NM_001375634.1:c.55-11788A>G	NP_001362563.1:n.55-11788A>G
NM_001375635.1:c.55-11788A>G MANE Select	NP_001362564.1:n.55-11788A>G
NM_020240.3:c.55-11788A>G	NP_064625.1:n.55-11788A>G