Canonical Allele Identifier: CA1153832227

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847298G= , CM000663.2:g.11847298G= GRCh38
NC_000001.10:g.11907355G= , CM000663.1:g.11907355G= GRCh37
NC_000001.9:g.11829942G= NCBI36
NG_012926.1:g.5486C= , LRG_751:g.5486C=

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1962-279G= (CLCN6) ENSP00000496938.1:n.*1962-279G=
ENST00000446542.5:n.782-136G= (NPPA-AS1)
ENST00000376476.1:c.115C= (NPPA) ENSP00000365659.1:p.Pro39=
ENST00000376480.7:c.265C= (NPPA) MANE Select ENSP00000365663.3:p.Pro89=
ENST00000610706.1:c.265C= (NPPA) ENSP00000483195.1:p.Pro89=
NM_006172.3:c.265C= , LRG_751t1:c.265C= (NPPA) NP_006163.1:p.Pro89=
NR_037806.1:n.1480-136G= (NPPA-AS1)
NM_006172.4:c.265C= (NPPA) MANE Select NP_006163.1:p.Pro89=