Canonical Allele Identifier: CA1153814197

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847684T= , CM000663.2:g.11847684T= GRCh38
NC_000001.10:g.11907741T= , CM000663.1:g.11907741T= GRCh37
NC_000001.9:g.11830328T= NCBI36
NG_012926.1:g.5100A= , LRG_751:g.5100A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*2069T= (CLCN6) ENSP00000496938.1:n.*2069T=
ENST00000446542.5:n.1032T= (NPPA-AS1)
ENST00000376476.1:c.-27-245A= (NPPA) ENSP00000365659.1:n.-27-245A=
ENST00000376480.7:c.1A= (NPPA) MANE Select ENSP00000365663.3:p.Met1=
ENST00000610706.1:c.1A= (NPPA) ENSP00000483195.1:p.Met1=
NM_006172.3:c.1A= , LRG_751t1:c.1A= (NPPA) NP_006163.1:p.Met1=
NM_006172.4:c.1A= (NPPA) MANE Select NP_006163.1:p.Met1=