Canonical Allele Identifier: CA1930506384
Gene: HOGA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97599793C= , CM000672.2:g.97599793C= GRCh38
NC_000010.10:g.99359550C= , CM000672.1:g.99359550C= GRCh37
NC_000010.9:g.99349540C= NCBI36
NG_027922.1:g.20449C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.582C= MANE Select ENSP00000359680.4:p.Gly194=
ENST00000370646.8:c.582C= ENSP00000359680.4:p.Gly194=
ENST00000370647.8:c.212-2064C= ENSP00000359681.4:n.212-2064C=
ENST00000370649.3:c.212-2064C= ENSP00000359683.3:n.212-2064C=
ENST00000465608.1:n.1426C=
NM_001134670.1:c.212-2064C= NP_001128142.1:n.212-2064C=
NM_138413.3:c.582C= NP_612422.2:p.Gly194=
NM_138413.4:c.582C= MANE Select NP_612422.2:p.Gly194=
NM_001134670.2:c.212-2064C= NP_001128142.1:n.212-2064C=