Canonical Allele Identifier: CA338451239

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847370C>G , CM000663.2:g.11847370C>G GRCh38
NC_000001.10:g.11907427C>G , CM000663.1:g.11907427C>G GRCh37
NC_000001.9:g.11830014C>G NCBI36
NG_012926.1:g.5414G>C , LRG_751:g.5414G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1962-207C>G (CLCN6) ENSP00000496938.1:n.*1962-207C>G
ENST00000446542.5:n.782-64C>G (NPPA-AS1)
ENST00000376476.1:c.43G>C (NPPA) ENSP00000365659.1:p.Glu15Gln
ENST00000376480.7:c.193G>C (NPPA) MANE Select ENSP00000365663.3:p.Glu65Gln
ENST00000610706.1:c.193G>C (NPPA) ENSP00000483195.1:p.Glu65Gln
NM_006172.3:c.193G>C , LRG_751t1:c.193G>C (NPPA) NP_006163.1:p.Glu65Gln
NR_037806.1:n.1480-64C>G (NPPA-AS1)
NM_006172.4:c.193G>C (NPPA) MANE Select NP_006163.1:p.Glu65Gln