Canonical Allele Identifier: CA670425519
Gene: HOGA1 HGNC NCBI

Linked Data

dbSNP Id: rs1162827379
gnomAD v3: 10-97611166-A-AC
gnomAD v4: 10-97611166-A-AC
MyVariant Identifiers: chr10:g.99370923_99370924insC (hg19) chr10:g.97611166_97611167insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97611167dup , CM000672.2:g.97611167dup GRCh38
NC_000010.10:g.99370924dup , CM000672.1:g.99370924dup GRCh37
NC_000010.9:g.99360914dup NCBI36
NG_027922.1:g.31823dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.835-343dup MANE Select ENSP00000359680.4:n.835-343dup
ENST00000370646.8:c.835-343dup ENSP00000359680.4:n.835-343dup
ENST00000370647.8:c.346-343dup ENSP00000359681.4:n.346-343dup
ENST00000370649.3:c.345+9177dup ENSP00000359683.3:n.345+9177dup
NM_001134670.1:c.346-343dup NP_001128142.1:n.346-343dup
NM_138413.3:c.835-343dup NP_612422.2:n.835-343dup
NM_138413.4:c.835-343dup MANE Select NP_612422.2:n.835-343dup
NM_001134670.2:c.346-343dup NP_001128142.1:n.346-343dup
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