ClinVar

NM_000018.4(ACADVL):c.1434+20G>A

Gene:

ACADVL:acyl-CoA dehydrogenase very long chain [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17p13.1

Genomic location:

• Chr17: 7224089 (on Assembly GRCh38)
• Chr17: 7127408 (on Assembly GRCh37)

Preferred name:

NM_000018.4(ACADVL):c.1434+20G>A

HGVS:

• NC_000017.11:g.7224089G>A
• NG_007975.1:g.9256G>A
• NG_008391.2:g.962C>T
• NG_008391.3:g.961C>T
• NG_033038.1:g.15456C>T
• NM_000018.4:c.1434+20G>AMANE SELECT
• NM_001033859.3:c.1368+20G>A
• NM_001270447.2:c.1503+20G>A
• NM_001270448.2:c.1206+20G>A
• NC_000017.10:g.7127408G>A

This HGVS expression did not pass validation

Molecular consequence:

• NM_000018.4:c.1434+20G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001033859.3:c.1368+20G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001270447.2:c.1503+20G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001270448.2:c.1206+20G>A - intron variant - [Sequence Ontology: SO:0001627]