ClinVar

NM_002667.5(PLN):c.45C>A (p.Ala15=)

Genes:

CEP85L:centrosomal protein 85 like [Gene - OMIM - HGNC]
PLN:phospholamban [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6q22.31

Genomic location:

• Chr6: 118558966 (on Assembly GRCh38)
• Chr6: 118880129 (on Assembly GRCh37)

Preferred name:

NM_002667.5(PLN):c.45C>A (p.Ala15=)

HGVS:

• NC_000006.12:g.118558966C>A
• NG_009082.1:g.15688C>A
• NG_021248.1:g.156110G>T
• NM_001042475.3:c.1020+6563G>TMANE SELECT
• NM_001178035.2:c.1029+6563G>T
• NM_002667.5:c.45C>AMANE SELECT
• NM_206921.3:c.1020+6563G>T
• NP_002658.1:p.Ala15=
• NP_002658.1:p.Ala15=
• LRG_390t1:c.45C>A
• LRG_390:g.15688C>A
• LRG_390p1:p.Ala15=
• NC_000006.11:g.118880129C>A
• NM_002667.3:c.45C>A

This HGVS expression did not pass validation

Molecular consequence:

• NM_001042475.3:c.1020+6563G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001178035.2:c.1029+6563G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_206921.3:c.1020+6563G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_002667.5:c.45C>A - synonymous variant - [Sequence Ontology: SO:0001819]