Canonical Allele Identifier: CA1930506819
Gene: HOGA1 HGNC NCBI

Linked Data

dbSNP Id: rs2041193336

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97611233del , CM000672.2:g.97611233del GRCh38
NC_000010.10:g.99370990del , CM000672.1:g.99370990del GRCh37
NC_000010.9:g.99360980del NCBI36
NG_027922.1:g.31889del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.835-277del MANE Select ENSP00000359680.4:n.835-277del
ENST00000370646.8:c.835-277del ENSP00000359680.4:n.835-277del
ENST00000370647.8:c.346-277del ENSP00000359681.4:n.346-277del
ENST00000370649.3:c.345+9243del ENSP00000359683.3:n.345+9243del
NM_001134670.1:c.346-277del NP_001128142.1:n.346-277del
NM_138413.3:c.835-277del NP_612422.2:n.835-277del
NM_138413.4:c.835-277del MANE Select NP_612422.2:n.835-277del
NM_001134670.2:c.346-277del NP_001128142.1:n.346-277del