Canonical Allele Identifier: CA203957
Gene: HOGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 204274
ClinVar RCV Id: RCV000186481
dbSNP Id: rs796052085
MyVariant Identifiers: chr10:g.99361641C>A (hg19) chr10:g.97601884C>A (hg38)
PubMed: PMID:22781098
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97601884C>A , CM000672.2:g.97601884C>A GRCh38
NC_000010.10:g.99361641C>A , CM000672.1:g.99361641C>A GRCh37
NC_000010.9:g.99351631C>A NCBI36
NG_027922.1:g.22540C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370646.9:c.728C>A MANE Select ENSP00000359680.4:p.Ala243Asp
ENST00000370642.4:c.138C>A
ENST00000370646.8:c.728C>A ENSP00000359680.4:p.Ala243Asp
ENST00000370647.8:c.239C>A ENSP00000359681.4:p.Ala80Asp
ENST00000370649.3:c.239C>A ENSP00000359683.3:p.Ala80Asp
NM_001134670.1:c.239C>A NP_001128142.1:p.Ala80Asp
NM_138413.3:c.728C>A NP_612422.2:p.Ala243Asp
NM_138413.4:c.728C>A MANE Select NP_612422.2:p.Ala243Asp
NM_001134670.2:c.239C>A NP_001128142.1:p.Ala80Asp
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