Canonical Allele Identifier: CA7361076

Gene: CDC42BPB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102967097T>C , CM000676.2:g.102967097T>C	GRCh38
NC_000014.8:g.103433434T>C , CM000676.1:g.103433434T>C	GRCh37
NC_000014.7:g.102503187T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559043.2:c.2420A>G	ENSP00000453384.2:p.Lys807Arg
ENST00000361246.7:c.2420A>G MANE Select	ENSP00000355237.2:p.Lys807Arg
ENST00000361246.6:c.2420A>G	ENSP00000355237.2:p.Lys807Arg
ENST00000559043.1:c.241A>G
NM_006035.3:c.2420A>G	NP_006026.3:p.Lys807Arg
XM_005268227.1:c.2420A>G	XP_005268284.1:p.Lys807Arg
XM_005268228.1:c.2420A>G	XP_005268285.1:p.Lys807Arg
XM_005268229.1:c.2420A>G	XP_005268286.1:p.Lys807Arg
XM_005268230.3:c.2420A>G	XP_005268287.1:p.Lys807Arg
XM_011537387.1:c.2420A>G	XP_011535689.1:p.Lys807Arg
XR_943564.1:n.2482A>G
XM_005268230.4:c.2420A>G	XP_005268287.1:p.Lys807Arg
NM_006035.4:c.2420A>G MANE Select	NP_006026.3:p.Lys807Arg