Canonical Allele Identifier: CA2088943280
Gene: CPB2 HGNC NCBI
CPB2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46055687_46055688delinsAC , CM000675.2:g.46055687_46055688delinsAC GRCh38
NC_000013.10:g.46629822_46629823delinsAC , CM000675.1:g.46629822_46629823delinsAC GRCh37
NC_000013.9:g.45527823_45527824delinsAC NCBI36
NG_032893.1:g.54389_54390delinsGT
NG_032893.2:g.54346_54347delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000181383.10:c.1087+74_1087+75delinsGT (CPB2) MANE Select ENSP00000181383.4:n.1087+74_1087+75delinsGT
ENST00000439329.5:c.976+74_976+75delinsGT (CPB2) ENSP00000400714.3:n.976+74_976+75delinsGT
ENST00000675730.1:c.*219+74_*219+75delinsGT (CPB2) ENSP00000502038.1:n.*219+74_*219+75delinsGT
ENST00000181383.8:c.1087+74_1087+75delinsGT (CPB2) ENSP00000181383.4:n.1087+74_1087+75delinsGT
ENST00000439329.4:c.976+74_976+75delinsGT (CPB2) ENSP00000400714.3:n.976+74_976+75delinsGT
NM_001278541.1:c.976+74_976+75delinsGT (CPB2) NP_001265470.1:n.976+74_976+75delinsGT
NM_001872.4:c.1087+74_1087+75delinsGT (CPB2) NP_001863.3:n.1087+74_1087+75delinsGT
NR_046226.1:n.118+2722_118+2723delinsAC (CPB2-AS1)
NR_046227.1:n.118+2722_118+2723delinsAC (CPB2-AS1)
XM_017020393.2:c.1060+74_1060+75delinsGT (CPB2) XP_016875882.1:n.1060+74_1060+75delinsGT
NM_001872.5:c.1087+74_1087+75delinsGT (CPB2) MANE Select NP_001863.3:n.1087+74_1087+75delinsGT
NM_001278541.2:c.976+74_976+75delinsGT (CPB2) NP_001265470.1:n.976+74_976+75delinsGT