Canonical Allele Identifier: CA2622928039

Gene: CPB2 CPB2-AS1

Linked Data

• gnomAD v4: 13-46055664-TATTTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46055668_46055672del , CM000675.2:g.46055668_46055672del	GRCh38
NC_000013.10:g.46629803_46629807del , CM000675.1:g.46629803_46629807del	GRCh37
NC_000013.9:g.45527804_45527808del	NCBI36
NG_032893.1:g.54408_54412del
NG_032893.2:g.54365_54369del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181383.10:c.1087+93_1087+97del (CPB2) MANE Select	ENSP00000181383.4:n.1087+93_1087+97del
ENST00000439329.5:c.976+93_976+97del (CPB2)	ENSP00000400714.3:n.976+93_976+97del
ENST00000675730.1:c.*219+93_*219+97del (CPB2)	ENSP00000502038.1:n.*219+93_*219+97del
ENST00000181383.8:c.1087+93_1087+97del (CPB2)	ENSP00000181383.4:n.1087+93_1087+97del
ENST00000439329.4:c.976+93_976+97del (CPB2)	ENSP00000400714.3:n.976+93_976+97del
NM_001278541.1:c.976+93_976+97del (CPB2)	NP_001265470.1:n.976+93_976+97del
NM_001872.4:c.1087+93_1087+97del (CPB2)	NP_001863.3:n.1087+93_1087+97del
NR_046226.1:n.118+2703_118+2707del (CPB2-AS1)
NR_046227.1:n.118+2703_118+2707del (CPB2-AS1)
XM_017020393.2:c.1060+93_1060+97del (CPB2)	XP_016875882.1:n.1060+93_1060+97del
NM_001872.5:c.1087+93_1087+97del (CPB2) MANE Select	NP_001863.3:n.1087+93_1087+97del
NM_001278541.2:c.976+93_976+97del (CPB2)	NP_001265470.1:n.976+93_976+97del