Canonical Allele Identifier: CA1153832032

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847204G= , CM000663.2:g.11847204G= GRCh38
NC_000001.10:g.11907261G= , CM000663.1:g.11907261G= GRCh37
NC_000001.9:g.11829848G= NCBI36
NG_012926.1:g.5580C= , LRG_751:g.5580C=

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1962-373G= (CLCN6) ENSP00000496938.1:n.*1962-373G=
ENST00000446542.5:n.782-230G= (NPPA-AS1)
ENST00000376476.1:c.209C= (NPPA) ENSP00000365659.1:p.Thr70=
ENST00000376480.7:c.359C= (NPPA) MANE Select ENSP00000365663.3:p.Thr120=
ENST00000610706.1:c.359C= (NPPA) ENSP00000483195.1:p.Thr120=
NM_006172.3:c.359C= , LRG_751t1:c.359C= (NPPA) NP_006163.1:p.Thr120=
NR_037806.1:n.1480-230G= (NPPA-AS1)
NM_006172.4:c.359C= (NPPA) MANE Select NP_006163.1:p.Thr120=