Canonical Allele Identifier: CA2160098388

Gene: CDC42BPB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103018488T= , CM000676.2:g.103018488T=	GRCh38
NC_000014.8:g.103484825T= , CM000676.1:g.103484825T=	GRCh37
NC_000014.7:g.102554578T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006035.4:c.176-6300A= MANE Select	NP_006026.3:n.176-6300A=
ENST00000361246.7:c.176-6300A= MANE Select	ENSP00000355237.2:n.176-6300A=
NM_006035.3:c.176-6300A=	NP_006026.3:n.176-6300A=
ENST00000361246.6:c.176-6300A=	ENSP00000355237.2:n.176-6300A=
ENST00000559043.2:c.176-6300A=	ENSP00000453384.2:n.176-6300A=
XM_005268227.1:c.176-6300A=	XP_005268284.1:n.176-6300A=
XM_005268228.1:c.176-6300A=	XP_005268285.1:n.176-6300A=
XM_005268229.1:c.176-6300A=	XP_005268286.1:n.176-6300A=
XM_005268230.3:c.176-6300A=	XP_005268287.1:n.176-6300A=
XM_005268230.4:c.176-6300A=	XP_005268287.1:n.176-6300A=
XM_011537387.1:c.176-6300A=	XP_011535689.1:n.176-6300A=
XR_943564.1:n.238-6300A=