Canonical Allele Identifier: CA1930507072
Gene: HOGA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97611588C= , CM000672.2:g.97611588C= GRCh38
NC_000010.10:g.99371345C= , CM000672.1:g.99371345C= GRCh37
NC_000010.9:g.99361335C= NCBI36
NG_027922.1:g.32244C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370646.9:c.913C= MANE Select ENSP00000359680.4:p.Pro305=
ENST00000370646.8:c.913C= ENSP00000359680.4:p.Pro305=
ENST00000370647.8:c.424C= ENSP00000359681.4:p.Pro142=
ENST00000370649.3:c.345+9598C= ENSP00000359683.3:n.345+9598C=
NM_001134670.1:c.424C= NP_001128142.1:p.Pro142=
NM_138413.3:c.913C= NP_612422.2:p.Pro305=
NM_138413.4:c.913C= MANE Select NP_612422.2:p.Pro305=
NM_001134670.2:c.424C= NP_001128142.1:p.Pro142=