Canonical Allele Identifier: CA212673182

Gene: HOGA1

Linked Data

• ClinVar Variation Id: 2909854
• ClinVar RCV Id: RCV003732479
• dbSNP Id: rs555444979
• gnomAD v3: 10-97599830-T-A
• gnomAD v4: 10-97599830-T-A
• MyVariant Identifiers: chr10:g.99359587T>A (hg19) ; chr10:g.97599830T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97599830T>A , CM000672.2:g.97599830T>A	GRCh38
NC_000010.10:g.99359587T>A , CM000672.1:g.99359587T>A	GRCh37
NC_000010.9:g.99349577T>A	NCBI36
NG_027922.1:g.20486T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.603+16T>A MANE Select	ENSP00000359680.4:n.603+16T>A
ENST00000370642.4:c.13+16T>A
ENST00000370646.8:c.603+16T>A	ENSP00000359680.4:n.603+16T>A
ENST00000370647.8:c.212-2027T>A	ENSP00000359681.4:n.212-2027T>A
ENST00000370649.3:c.212-2027T>A	ENSP00000359683.3:n.212-2027T>A
ENST00000465608.1:n.1463T>A
NM_001134670.1:c.212-2027T>A	NP_001128142.1:n.212-2027T>A
NM_138413.3:c.603+16T>A	NP_612422.2:n.603+16T>A
NM_138413.4:c.603+16T>A MANE Select	NP_612422.2:n.603+16T>A
NM_001134670.2:c.212-2027T>A	NP_001128142.1:n.212-2027T>A