Canonical Allele Identifier: CA1930506978
Gene: HOGA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97600189G= , CM000672.2:g.97600189G= GRCh38
NC_000010.10:g.99359946G= , CM000672.1:g.99359946G= GRCh37
NC_000010.9:g.99349936G= NCBI36
NG_027922.1:g.20845G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370646.9:c.700+26G= MANE Select ENSP00000359680.4:n.700+26G=
ENST00000370642.4:c.110+26G=
ENST00000370646.8:c.700+26G= ENSP00000359680.4:n.700+26G=
ENST00000370647.8:c.212-1668G= ENSP00000359681.4:n.212-1668G=
ENST00000370649.3:c.212-1668G= ENSP00000359683.3:n.212-1668G=
ENST00000465608.1:n.1822G=
NM_001134670.1:c.212-1668G= NP_001128142.1:n.212-1668G=
NM_138413.3:c.700+26G= NP_612422.2:n.700+26G=
NM_138413.4:c.700+26G= MANE Select NP_612422.2:n.700+26G=
NM_001134670.2:c.212-1668G= NP_001128142.1:n.212-1668G=