Canonical Allele Identifier: CA1930504862
Gene: HOGA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97598874G= , CM000672.2:g.97598874G= GRCh38
NC_000010.10:g.99358631G= , CM000672.1:g.99358631G= GRCh37
NC_000010.9:g.99348621G= NCBI36
NG_027922.1:g.19530G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370646.9:c.311G= MANE Select ENSP00000359680.4:p.Arg104=
ENST00000370646.8:c.311G= ENSP00000359680.4:p.Arg104=
ENST00000370647.8:c.212-2983G= ENSP00000359681.4:n.212-2983G=
ENST00000370649.3:c.212-2983G= ENSP00000359683.3:n.212-2983G=
ENST00000465608.1:n.692G=
NM_001134670.1:c.212-2983G= NP_001128142.1:n.212-2983G=
NM_138413.3:c.311G= NP_612422.2:p.Arg104=
NM_138413.4:c.311G= MANE Select NP_612422.2:p.Arg104=
NM_001134670.2:c.212-2983G= NP_001128142.1:n.212-2983G=