Canonical Allele Identifier: CA1930504928
Gene: HOGA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97598901A= , CM000672.2:g.97598901A= GRCh38
NC_000010.10:g.99358658A= , CM000672.1:g.99358658A= GRCh37
NC_000010.9:g.99348648A= NCBI36
NG_027922.1:g.19557A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.338A= MANE Select ENSP00000359680.4:p.Glu113=
ENST00000370646.8:c.338A= ENSP00000359680.4:p.Glu113=
ENST00000370647.8:c.212-2956A= ENSP00000359681.4:n.212-2956A=
ENST00000370649.3:c.212-2956A= ENSP00000359683.3:n.212-2956A=
ENST00000465608.1:n.719A=
NM_001134670.1:c.212-2956A= NP_001128142.1:n.212-2956A=
NM_138413.3:c.338A= NP_612422.2:p.Glu113=
NM_138413.4:c.338A= MANE Select NP_612422.2:p.Glu113=
NM_001134670.2:c.212-2956A= NP_001128142.1:n.212-2956A=
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