Canonical Allele Identifier: CA2634848278
Community Standard Title: NM_000101.4(CYBA):c.467del (p.Pro156ArgfsTer?)
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643479del , CM000678.2:g.88643479del GRCh38
NC_000016.9:g.88709887del , CM000678.1:g.88709887del GRCh37
NC_000016.8:g.87237388del NCBI36
NG_007291.1:g.12576del , LRG_52:g.12576del

Transcript Alleles

HGVS Amino-acid Change
NM_000101.4:c.467del MANE Select NP_000092.2:p.Pro156ArgfsTer?
ENST00000261623.8:c.467del MANE Select ENSP00000261623.3:p.Pro156ArgfsTer?
NM_000101.3:c.467del NP_000092.2:p.Pro156ArgfsTer?
ENST00000261623.7:c.467del ENSP00000261623.3:p.Pro156ArgfsTer?
ENST00000696156.1:c.383del ENSP00000512446.1:p.Pro128ArgfsTer?
ENST00000696157.1:c.*684del ENSP00000512447.1:n.*684del
ENST00000696158.1:c.*721del ENSP00000512448.1:n.*721del
ENST00000696159.1:c.*390del ENSP00000512449.1:n.*390del
ENST00000696160.1:c.494del ENSP00000512450.1:p.Pro165ArgfsTer?
ENST00000696161.1:c.597del ENSP00000512451.1:p.Ala200ProfsTer?
ENST00000696162.1:c.*1186del ENSP00000512452.1:n.*1186del
ENST00000696163.1:c.416del ENSP00000512453.1:p.Pro139ArgfsTer?