Canonical Allele Identifier: CA2502508057

Gene: CPB2 CPB2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46055647_46055648insATTGAGGC , CM000675.2:g.46055647_46055648insATTGAGGC	GRCh38
NC_000013.10:g.46629782_46629783insATTGAGGC , CM000675.1:g.46629782_46629783insATTGAGGC	GRCh37
NC_000013.9:g.45527783_45527784insATTGAGGC	NCBI36
NG_032893.1:g.54429_54430insGCCTCAAT
NG_032893.2:g.54386_54387insGCCTCAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181383.10:c.1087+114_1087+115insGCCTCAAT (CPB2) MANE Select	ENSP00000181383.4:n.1087+114_1087+115insGCCTCAAT
ENST00000439329.5:c.976+114_976+115insGCCTCAAT (CPB2)	ENSP00000400714.3:n.976+114_976+115insGCCTCAAT
ENST00000675730.1:c.*219+114_*219+115insGCCTCAAT (CPB2)	ENSP00000502038.1:n.*219+114_*219+115insGCCTCAAT
ENST00000181383.8:c.1087+114_1087+115insGCCTCAAT (CPB2)	ENSP00000181383.4:n.1087+114_1087+115insGCCTCAAT
ENST00000439329.4:c.976+114_976+115insGCCTCAAT (CPB2)	ENSP00000400714.3:n.976+114_976+115insGCCTCAAT
NM_001278541.1:c.976+114_976+115insGCCTCAAT (CPB2)	NP_001265470.1:n.976+114_976+115insGCCTCAAT
NM_001872.4:c.1087+114_1087+115insGCCTCAAT (CPB2)	NP_001863.3:n.1087+114_1087+115insGCCTCAAT
NR_046226.1:n.118+2682_118+2683insATTGAGGC (CPB2-AS1)
NR_046227.1:n.118+2682_118+2683insATTGAGGC (CPB2-AS1)
XM_017020393.2:c.1060+114_1060+115insGCCTCAAT (CPB2)	XP_016875882.1:n.1060+114_1060+115insGCCTCAAT
NM_001872.5:c.1087+114_1087+115insGCCTCAAT (CPB2) MANE Select	NP_001863.3:n.1087+114_1087+115insGCCTCAAT
NM_001278541.2:c.976+114_976+115insGCCTCAAT (CPB2)	NP_001265470.1:n.976+114_976+115insGCCTCAAT