Canonical Allele Identifier: CA1582690864

Gene: CDC42SE2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.131373630T= , CM000667.2:g.131373630T=	GRCh38
NC_000005.9:g.130709323T= , CM000667.1:g.130709323T=	GRCh37
NC_000005.8:g.130737222T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505065.2:c.55-11913T= MANE Select	ENSP00000427421.1:n.55-11913T=
ENST00000360515.7:c.55-11913T=	ENSP00000353706.3:n.55-11913T=
ENST00000395246.5:c.55-11913T=	ENSP00000378667.1:n.55-11913T=
ENST00000503291.5:c.-27-11913T=	ENSP00000426779.1:n.-27-11913T=
ENST00000505065.1:c.55-11913T=	ENSP00000427421.1:n.55-11913T=
NM_001038702.1:c.55-11913T=	NP_001033791.1:n.55-11913T=
NM_020240.2:c.55-11913T=	NP_064625.1:n.55-11913T=
XM_017009648.2:c.55-11913T=	XP_016865137.1:n.55-11913T=
XM_017009649.2:c.55-11913T=	XP_016865138.1:n.55-11913T=
NM_001038702.2:c.55-11913T=	NP_001033791.1:n.55-11913T=
NM_001375633.1:c.55-11913T=	NP_001362562.1:n.55-11913T=
NM_001375634.1:c.55-11913T=	NP_001362563.1:n.55-11913T=
NM_001375635.1:c.55-11913T= MANE Select	NP_001362564.1:n.55-11913T=
NM_020240.3:c.55-11913T=	NP_064625.1:n.55-11913T=