Canonical Allele Identifier: CA5634050
Gene: HOGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 397590
ClinVar RCV Id: RCV000449564
dbSNP Id: rs200529020

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97598894G>A , CM000672.2:g.97598894G>A GRCh38
NC_000010.10:g.99358651G>A , CM000672.1:g.99358651G>A GRCh37
NC_000010.9:g.99348641G>A NCBI36
NG_027922.1:g.19550G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.331G>A MANE Select ENSP00000359680.4:p.Gly111Arg
ENST00000370646.8:c.331G>A ENSP00000359680.4:p.Gly111Arg
ENST00000370647.8:c.212-2963G>A ENSP00000359681.4:n.212-2963G>A
ENST00000370649.3:c.212-2963G>A ENSP00000359683.3:n.212-2963G>A
ENST00000465608.1:n.712G>A
NM_001134670.1:c.212-2963G>A NP_001128142.1:n.212-2963G>A
NM_138413.3:c.331G>A NP_612422.2:p.Gly111Arg
NM_138413.4:c.331G>A MANE Select NP_612422.2:p.Gly111Arg
NM_001134670.2:c.212-2963G>A NP_001128142.1:n.212-2963G>A