Canonical Allele Identifier: CA1930506396
Gene: HOGA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97599798A= , CM000672.2:g.97599798A= GRCh38
NC_000010.10:g.99359555A= , CM000672.1:g.99359555A= GRCh37
NC_000010.9:g.99349545A= NCBI36
NG_027922.1:g.20454A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.587A= MANE Select ENSP00000359680.4:p.Lys196=
ENST00000370646.8:c.587A= ENSP00000359680.4:p.Lys196=
ENST00000370647.8:c.212-2059A= ENSP00000359681.4:n.212-2059A=
ENST00000370649.3:c.212-2059A= ENSP00000359683.3:n.212-2059A=
ENST00000465608.1:n.1431A=
NM_001134670.1:c.212-2059A= NP_001128142.1:n.212-2059A=
NM_138413.3:c.587A= NP_612422.2:p.Lys196=
NM_138413.4:c.587A= MANE Select NP_612422.2:p.Lys196=
NM_001134670.2:c.212-2059A= NP_001128142.1:n.212-2059A=