Canonical Allele Identifier: CA338450555

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847300C>G , CM000663.2:g.11847300C>G GRCh38
NC_000001.10:g.11907357C>G , CM000663.1:g.11907357C>G GRCh37
NC_000001.9:g.11829944C>G NCBI36
NG_012926.1:g.5484G>C , LRG_751:g.5484G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1962-277C>G (CLCN6) ENSP00000496938.1:n.*1962-277C>G
ENST00000446542.5:n.782-134C>G (NPPA-AS1)
ENST00000376476.1:c.113G>C (NPPA) ENSP00000365659.1:p.Ser38Thr
ENST00000376480.7:c.263G>C (NPPA) MANE Select ENSP00000365663.3:p.Ser88Thr
ENST00000610706.1:c.263G>C (NPPA) ENSP00000483195.1:p.Ser88Thr
NM_006172.3:c.263G>C , LRG_751t1:c.263G>C (NPPA) NP_006163.1:p.Ser88Thr
NR_037806.1:n.1480-134C>G (NPPA-AS1)
NM_006172.4:c.263G>C (NPPA) MANE Select NP_006163.1:p.Ser88Thr