Canonical Allele Identifier: CA5634168

Gene: HOGA1

Linked Data

• ClinVar Variation Id: 2749061
• ClinVar RCV Id: RCV003566284
• dbSNP Id: rs113921655
• ExAC: 10:99359584 A / G
• gnomAD v2: 10-99359584-A-G
• gnomAD v3: 10-97599827-A-G
• gnomAD v4: 10-97599827-A-G
• MyVariant Identifiers: chr10:g.99359584A>G (hg19) ; chr10:g.97599827A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97599827A>G , CM000672.2:g.97599827A>G	GRCh38
NC_000010.10:g.99359584A>G , CM000672.1:g.99359584A>G	GRCh37
NC_000010.9:g.99349574A>G	NCBI36
NG_027922.1:g.20483A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.603+13A>G MANE Select	ENSP00000359680.4:n.603+13A>G
ENST00000370642.4:c.13+13A>G
ENST00000370646.8:c.603+13A>G	ENSP00000359680.4:n.603+13A>G
ENST00000370647.8:c.212-2030A>G	ENSP00000359681.4:n.212-2030A>G
ENST00000370649.3:c.212-2030A>G	ENSP00000359683.3:n.212-2030A>G
ENST00000465608.1:n.1460A>G
NM_001134670.1:c.212-2030A>G	NP_001128142.1:n.212-2030A>G
NM_138413.3:c.603+13A>G	NP_612422.2:n.603+13A>G
NM_138413.4:c.603+13A>G MANE Select	NP_612422.2:n.603+13A>G
NM_001134670.2:c.212-2030A>G	NP_001128142.1:n.212-2030A>G