Canonical Allele Identifier: CA7360364

Gene: CDC42BPB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102939944G>A , CM000676.2:g.102939944G>A	GRCh38
NC_000014.8:g.103406281G>A , CM000676.1:g.103406281G>A	GRCh37
NC_000014.7:g.102476034G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006035.4:c.4595C>T MANE Select	NP_006026.3:p.Ala1532Val
ENST00000361246.7:c.4595C>T MANE Select	ENSP00000355237.2:p.Ala1532Val
NM_006035.3:c.4595C>T	NP_006026.3:p.Ala1532Val
ENST00000361246.6:c.4595C>T	ENSP00000355237.2:p.Ala1532Val
ENST00000559043.2:c.4517C>T	ENSP00000453384.2:p.Ala1506Val
ENST00000559790.1:n.685C>T
ENST00000560492.1:n.610C>T
XM_005268227.1:c.4646C>T	XP_005268284.1:p.Ala1549Val
XM_005268228.1:c.4568C>T	XP_005268285.1:p.Ala1523Val
XM_005268229.1:c.4517C>T	XP_005268286.1:p.Ala1506Val
XR_943564.1:n.4524C>T