Canonical Allele Identifier: CA1153832229

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847299G= , CM000663.2:g.11847299G= GRCh38
NC_000001.10:g.11907356G= , CM000663.1:g.11907356G= GRCh37
NC_000001.9:g.11829943G= NCBI36
NG_012926.1:g.5485C= , LRG_751:g.5485C=

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1962-278G= (CLCN6) ENSP00000496938.1:n.*1962-278G=
ENST00000446542.5:n.782-135G= (NPPA-AS1)
ENST00000376476.1:c.114C= (NPPA) ENSP00000365659.1:p.Ser38=
ENST00000376480.7:c.264C= (NPPA) MANE Select ENSP00000365663.3:p.Ser88=
ENST00000610706.1:c.264C= (NPPA) ENSP00000483195.1:p.Ser88=
NM_006172.3:c.264C= , LRG_751t1:c.264C= (NPPA) NP_006163.1:p.Ser88=
NR_037806.1:n.1480-135G= (NPPA-AS1)
NM_006172.4:c.264C= (NPPA) MANE Select NP_006163.1:p.Ser88=