Canonical Allele Identifier: CA267135586

Gene: CDC42BPB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102944131A>G , CM000676.2:g.102944131A>G	GRCh38
NC_000014.8:g.103410468A>G , CM000676.1:g.103410468A>G	GRCh37
NC_000014.7:g.102480221A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006035.4:c.4168T>C MANE Select	NP_006026.3:p.Tyr1390His
ENST00000361246.7:c.4168T>C MANE Select	ENSP00000355237.2:p.Tyr1390His
NM_006035.3:c.4168T>C	NP_006026.3:p.Tyr1390His
ENST00000361246.6:c.4168T>C	ENSP00000355237.2:p.Tyr1390His
ENST00000558867.1:n.515T>C
ENST00000559043.1:c.1911T>C
ENST00000559043.2:c.4090T>C	ENSP00000453384.2:p.Tyr1364His
ENST00000559245.1:n.420T>C
XM_005268227.1:c.4219T>C	XP_005268284.1:p.Tyr1407His
XM_005268228.1:c.4141T>C	XP_005268285.1:p.Tyr1381His
XM_005268229.1:c.4090T>C	XP_005268286.1:p.Tyr1364His
XM_005268230.3:c.4219T>C	XP_005268287.1:p.Tyr1407His
XM_005268230.4:c.4219T>C	XP_005268287.1:p.Tyr1407His
XM_011537387.1:c.4219T>C	XP_011535689.1:p.Tyr1407His
XR_943564.1:n.4281T>C