Canonical Allele Identifier: CA5634304
Gene: HOGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2241698
ClinVar RCV Id: RCV002767260
dbSNP Id: rs760180544
ExAC: 10:99371331 G / A
gnomAD v2: 10-99371331-G-A
gnomAD v4: 10-97611574-G-A
MyVariant Identifiers: chr10:g.99371331G>A (hg19) chr10:g.97611574G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97611574G>A , CM000672.2:g.97611574G>A GRCh38
NC_000010.10:g.99371331G>A , CM000672.1:g.99371331G>A GRCh37
NC_000010.9:g.99361321G>A NCBI36
NG_027922.1:g.32230G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.899G>A MANE Select ENSP00000359680.4:p.Gly300Asp
ENST00000370646.8:c.899G>A ENSP00000359680.4:p.Gly300Asp
ENST00000370647.8:c.410G>A ENSP00000359681.4:p.Gly137Asp
ENST00000370649.3:c.345+9584G>A ENSP00000359683.3:n.345+9584G>A
NM_001134670.1:c.410G>A NP_001128142.1:p.Gly137Asp
NM_138413.3:c.899G>A NP_612422.2:p.Gly300Asp
NM_138413.4:c.899G>A MANE Select NP_612422.2:p.Gly300Asp
NM_001134670.2:c.410G>A NP_001128142.1:p.Gly137Asp
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