ClinVar

NM_001352514.2(HLCS):c.703G>A (p.Asp235Asn)

Gene:

HLCS:holocarboxylase synthetase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

21q22.13

Genomic location:

• Chr21: 36937183 (on Assembly GRCh38)
• Chr21: 38309483 (on Assembly GRCh37)

Preferred name:

NM_001352514.2(HLCS):c.703G>A (p.Asp235Asn)

HGVS:

• NC_000021.9:g.36937183C>T
• NG_016193.2:g.58212G>A
• NM_000411.6:c.262G>A
• NM_000411.8:c.262G>A
• NM_001242784.3:c.262G>A
• NM_001242785.2:c.262G>A
• NM_001352514.2:c.703G>AMANE SELECT
• NM_001352515.2:c.262G>A
• NM_001352516.2:c.262G>A
• NM_001352517.1:c.262G>A
• NM_001352518.2:c.262G>A
• NP_000402.3:p.Asp88Asn
• NP_001229713.1:p.Asp88Asn
• NP_001229714.1:p.Asp88Asn
• NP_001339443.1:p.Asp235Asn
• NP_001339444.1:p.Asp88Asn
• NP_001339445.1:p.Asp88Asn
• NP_001339446.1:p.Asp88Asn
• NP_001339447.1:p.Asp88Asn
• NC_000021.8:g.38309483C>T
• NR_148020.2:n.562G>A
• NR_148021.1:n.719G>A

This HGVS expression did not pass validation

Protein change:

D235N

Links:

dbSNP: rs373951547

NCBI 1000 Genomes Browser:

rs373951547

Molecular consequence:

• NM_000411.8:c.262G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001242784.3:c.262G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001242785.2:c.262G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001352514.2:c.703G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001352515.2:c.262G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001352516.2:c.262G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001352517.1:c.262G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001352518.2:c.262G>A - missense variant - [Sequence Ontology: SO:0001583]
• NR_148020.2:n.562G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NR_148021.1:n.719G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]