ClinVar

NM_000390.4(CHM):c.528G>A (p.Gly176=)

Gene:

CHM:CHM Rab escort protein [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

Xq21.2

Genomic location:

• ChrX: 85963839 (on Assembly GRCh38)
• ChrX: 85218844 (on Assembly GRCh37)

Preferred name:

NM_000390.4(CHM):c.528G>A (p.Gly176=)

HGVS:

• NC_000023.11:g.85963839C>T
• NG_009874.2:g.88724G>A
• NM_000390.4:c.528G>AMANE SELECT
• NM_001320959.1:c.84G>A
• NM_001362517.1:c.84G>A
• NM_001362518.2:c.84G>A
• NM_001362519.1:c.84G>A
• NP_000381.1:p.Gly176=
• NP_001307888.1:p.Gly28=
• NP_001349446.1:p.Gly28=
• NP_001349447.1:p.Gly28=
• NP_001349448.1:p.Gly28=
• LRG_699:g.88724G>A
• NC_000023.10:g.85218844C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs753958657

NCBI 1000 Genomes Browser:

rs753958657

Molecular consequence:

• NM_000390.4:c.528G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001320959.1:c.84G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001362517.1:c.84G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001362518.2:c.84G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001362519.1:c.84G>A - synonymous variant - [Sequence Ontology: SO:0001819]