Canonical Allele Identifier: CA338450531

Linked Data

ClinVar Variation Id: 2871910
ClinVar RCV Id: RCV003632310

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847297G>T , CM000663.2:g.11847297G>T GRCh38
NC_000001.10:g.11907354G>T , CM000663.1:g.11907354G>T GRCh37
NC_000001.9:g.11829941G>T NCBI36
NG_012926.1:g.5487C>A , LRG_751:g.5487C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1962-280G>T (CLCN6) ENSP00000496938.1:n.*1962-280G>T
ENST00000446542.5:n.782-137G>T (NPPA-AS1)
ENST00000376476.1:c.116C>A (NPPA) ENSP00000365659.1:p.Pro39Gln
ENST00000376480.7:c.266C>A (NPPA) MANE Select ENSP00000365663.3:p.Pro89Gln
ENST00000610706.1:c.266C>A (NPPA) ENSP00000483195.1:p.Pro89Gln
NM_006172.3:c.266C>A , LRG_751t1:c.266C>A (NPPA) NP_006163.1:p.Pro89Gln
NR_037806.1:n.1480-137G>T (NPPA-AS1)
NM_006172.4:c.266C>A (NPPA) MANE Select NP_006163.1:p.Pro89Gln