Canonical Allele Identifier: CA203934
Gene: HOGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 204264
ClinVar RCV Id: RCV001520020
dbSNP Id: rs12261752
ExAC: 10:99371344 C / A
gnomAD v2: 10-99371344-C-A
gnomAD v3: 10-97611587-C-A
gnomAD v4: 10-97611587-C-A
MyVariant Identifiers: chr10:g.99371344C>A (hg19) chr10:g.97611587C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97611587C>A , CM000672.2:g.97611587C>A GRCh38
NC_000010.10:g.99371344C>A , CM000672.1:g.99371344C>A GRCh37
NC_000010.9:g.99361334C>A NCBI36
NG_027922.1:g.32243C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370646.9:c.912C>A MANE Select ENSP00000359680.4:p.Ala304=
ENST00000370646.8:c.912C>A ENSP00000359680.4:p.Ala304=
ENST00000370647.8:c.423C>A ENSP00000359681.4:p.Ala141=
ENST00000370649.3:c.345+9597C>A ENSP00000359683.3:n.345+9597C>A
NM_001134670.1:c.423C>A NP_001128142.1:p.Ala141=
NM_138413.3:c.912C>A NP_612422.2:p.Ala304=
NM_138413.4:c.912C>A MANE Select NP_612422.2:p.Ala304=
NM_001134670.2:c.423C>A NP_001128142.1:p.Ala141=
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