Canonical Allele Identifier: CA338449152

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847176G>C , CM000663.2:g.11847176G>C GRCh38
NC_000001.10:g.11907233G>C , CM000663.1:g.11907233G>C GRCh37
NC_000001.9:g.11829820G>C NCBI36
NG_012926.1:g.5608C>G , LRG_751:g.5608C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1962-401G>C (CLCN6) ENSP00000496938.1:n.*1962-401G>C
ENST00000446542.5:n.782-258G>C (NPPA-AS1)
ENST00000376476.1:c.237C>G (NPPA) ENSP00000365659.1:p.Ser79Arg
ENST00000376480.7:c.387C>G (NPPA) MANE Select ENSP00000365663.3:p.Ser129Arg
ENST00000610706.1:c.387C>G (NPPA) ENSP00000483195.1:p.Ser129Arg
NM_006172.3:c.387C>G , LRG_751t1:c.387C>G (NPPA) NP_006163.1:p.Ser129Arg
NR_037806.1:n.1480-258G>C (NPPA-AS1)
NM_006172.4:c.387C>G (NPPA) MANE Select NP_006163.1:p.Ser129Arg