Canonical Allele Identifier: CA2991005419

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847124del , CM000663.2:g.11847124del GRCh38
NC_000001.10:g.11907181del , CM000663.1:g.11907181del GRCh37
NC_000001.9:g.11829768del NCBI36
NG_012926.1:g.5661del , LRG_751:g.5661del

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1962-453del (CLCN6) ENSP00000496938.1:n.*1962-453del
ENST00000446542.5:n.782-310del (NPPA-AS1)
ENST00000376476.1:c.290del (NPPA) ENSP00000365659.1:p.Asn97ThrfsTer?
ENST00000376480.7:c.440del (NPPA) MANE Select ENSP00000365663.3:p.Asn147ThrfsTer?
ENST00000610706.1:c.440del (NPPA) ENSP00000483195.1:p.Asn147ThrfsTer?
NM_006172.3:c.440del , LRG_751t1:c.440del (NPPA) NP_006163.1:p.Asn147ThrfsTer?
NR_037806.1:n.1480-310del (NPPA-AS1)
NM_006172.4:c.440del (NPPA) MANE Select NP_006163.1:p.Asn147ThrfsTer?