Canonical Allele Identifier: CA2503994707

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11846945G>C , CM000663.2:g.11846945G>C GRCh38
NC_000001.10:g.11907002G>C , CM000663.1:g.11907002G>C GRCh37
NC_000001.9:g.11829589G>C NCBI36
NG_012926.1:g.5839C>G , LRG_751:g.5839C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1962-632G>C (CLCN6) ENSP00000496938.1:n.*1962-632G>C
ENST00000446542.5:n.782-489G>C (NPPA-AS1)
ENST00000376476.1:c.300+168C>G (NPPA) ENSP00000365659.1:n.300+168C>G
ENST00000376480.7:c.450+168C>G (NPPA) MANE Select ENSP00000365663.3:n.450+168C>G
ENST00000610706.1:c.450+168C>G (NPPA) ENSP00000483195.1:n.450+168C>G
NM_006172.3:c.450+168C>G , LRG_751t1:c.450+168C>G (NPPA) NP_006163.1:n.450+168C>G
NR_037806.1:n.1480-489G>C (NPPA-AS1)
NM_006172.4:c.450+168C>G (NPPA) MANE Select NP_006163.1:n.450+168C>G