Canonical Allele Identifier: CA471092771

Gene: HOGA1

Linked Data

• ClinVar Variation Id: 1102889
• ClinVar RCV Id: RCV001426349
• dbSNP Id: rs2135729850
• gnomAD v4: 10-97611569-T-C
• MyVariant Identifiers: chr10:g.99371326T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97611569T>C , CM000672.2:g.97611569T>C	GRCh38
NC_000010.10:g.99371326T>C , CM000672.1:g.99371326T>C	GRCh37
NC_000010.9:g.99361316T>C	NCBI36
NG_027922.1:g.32225T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.894T>C MANE Select	ENSP00000359680.4:p.Tyr298=
ENST00000370646.8:c.894T>C	ENSP00000359680.4:p.Tyr298=
ENST00000370647.8:c.405T>C	ENSP00000359681.4:p.Tyr135=
ENST00000370649.3:c.345+9579T>C	ENSP00000359683.3:n.345+9579T>C
NM_001134670.1:c.405T>C	NP_001128142.1:p.Tyr135=
NM_138413.3:c.894T>C	NP_612422.2:p.Tyr298=
NM_138413.4:c.894T>C MANE Select	NP_612422.2:p.Tyr298=
NM_001134670.2:c.405T>C	NP_001128142.1:p.Tyr135=