Canonical Allele Identifier: CA595408292

Gene: HOGA1

Linked Data

• ClinVar Variation Id: 2916674
• ClinVar RCV Id: RCV003740472
• dbSNP Id: rs1171792440
• gnomAD v2: 10-99359589-C-T
• gnomAD v4: 10-97599832-C-T
• MyVariant Identifiers: chr10:g.99359589C>T (hg19) ; chr10:g.97599832C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97599832C>T , CM000672.2:g.97599832C>T	GRCh38
NC_000010.10:g.99359589C>T , CM000672.1:g.99359589C>T	GRCh37
NC_000010.9:g.99349579C>T	NCBI36
NG_027922.1:g.20488C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.603+18C>T MANE Select	ENSP00000359680.4:n.603+18C>T
ENST00000370642.4:c.13+18C>T
ENST00000370646.8:c.603+18C>T	ENSP00000359680.4:n.603+18C>T
ENST00000370647.8:c.212-2025C>T	ENSP00000359681.4:n.212-2025C>T
ENST00000370649.3:c.212-2025C>T	ENSP00000359683.3:n.212-2025C>T
ENST00000465608.1:n.1465C>T
NM_001134670.1:c.212-2025C>T	NP_001128142.1:n.212-2025C>T
NM_138413.3:c.603+18C>T	NP_612422.2:n.603+18C>T
NM_138413.4:c.603+18C>T MANE Select	NP_612422.2:n.603+18C>T
NM_001134670.2:c.212-2025C>T	NP_001128142.1:n.212-2025C>T