Canonical Allele Identifier: CA7361359

Gene: CDC42BPB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102974136G>C , CM000676.2:g.102974136G>C	GRCh38
NC_000014.8:g.103440473G>C , CM000676.1:g.103440473G>C	GRCh37
NC_000014.7:g.102510226G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559043.2:c.1521C>G	ENSP00000453384.2:p.Leu507=
ENST00000361246.7:c.1521C>G MANE Select	ENSP00000355237.2:p.Leu507=
ENST00000361246.6:c.1521C>G	ENSP00000355237.2:p.Leu507=
NM_006035.3:c.1521C>G	NP_006026.3:p.Leu507=
XM_005268227.1:c.1521C>G	XP_005268284.1:p.Leu507=
XM_005268228.1:c.1521C>G	XP_005268285.1:p.Leu507=
XM_005268229.1:c.1521C>G	XP_005268286.1:p.Leu507=
XM_005268230.3:c.1521C>G	XP_005268287.1:p.Leu507=
XM_011537387.1:c.1521C>G	XP_011535689.1:p.Leu507=
XR_943564.1:n.1583C>G
XM_005268230.4:c.1521C>G	XP_005268287.1:p.Leu507=
NM_006035.4:c.1521C>G MANE Select	NP_006026.3:p.Leu507=