Canonical Allele Identifier: CA1930506971
Gene: HOGA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97611518G= , CM000672.2:g.97611518G= GRCh38
NC_000010.10:g.99371275G= , CM000672.1:g.99371275G= GRCh37
NC_000010.9:g.99361265G= NCBI36
NG_027922.1:g.32174G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.843G= MANE Select ENSP00000359680.4:p.Arg281=
ENST00000370646.8:c.843G= ENSP00000359680.4:p.Arg281=
ENST00000370647.8:c.354G= ENSP00000359681.4:p.Arg118=
ENST00000370649.3:c.345+9528G= ENSP00000359683.3:n.345+9528G=
NM_001134670.1:c.354G= NP_001128142.1:p.Arg118=
NM_138413.3:c.843G= NP_612422.2:p.Arg281=
NM_138413.4:c.843G= MANE Select NP_612422.2:p.Arg281=
NM_001134670.2:c.354G= NP_001128142.1:p.Arg118=