Canonical Allele Identifier: CA2088943295

Gene: CPB2 CPB2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46055721G= , CM000675.2:g.46055721G=	GRCh38
NC_000013.10:g.46629856G= , CM000675.1:g.46629856G=	GRCh37
NC_000013.9:g.45527857G=	NCBI36
NG_032893.1:g.54356C=
NG_032893.2:g.54313C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000181383.10:c.1087+41C= (CPB2) MANE Select	ENSP00000181383.4:n.1087+41C=
ENST00000439329.5:c.976+41C= (CPB2)	ENSP00000400714.3:n.976+41C=
ENST00000675730.1:c.*219+41C= (CPB2)	ENSP00000502038.1:n.*219+41C=
ENST00000181383.8:c.1087+41C= (CPB2)	ENSP00000181383.4:n.1087+41C=
ENST00000439329.4:c.976+41C= (CPB2)	ENSP00000400714.3:n.976+41C=
NM_001278541.1:c.976+41C= (CPB2)	NP_001265470.1:n.976+41C=
NM_001872.4:c.1087+41C= (CPB2)	NP_001863.3:n.1087+41C=
NR_046226.1:n.118+2756G= (CPB2-AS1)
NR_046227.1:n.118+2756G= (CPB2-AS1)
XM_017020393.2:c.1060+41C= (CPB2)	XP_016875882.1:n.1060+41C=
NM_001872.5:c.1087+41C= (CPB2) MANE Select	NP_001863.3:n.1087+41C=
NM_001278541.2:c.976+41C= (CPB2)	NP_001265470.1:n.976+41C=