Canonical Allele Identifier: CA377983468
Gene: HOGA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.99371324T>A (hg19) chr10:g.97611567T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97611567T>A , CM000672.2:g.97611567T>A GRCh38
NC_000010.10:g.99371324T>A , CM000672.1:g.99371324T>A GRCh37
NC_000010.9:g.99361314T>A NCBI36
NG_027922.1:g.32223T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.892T>A MANE Select ENSP00000359680.4:p.Tyr298Asn
ENST00000370646.8:c.892T>A ENSP00000359680.4:p.Tyr298Asn
ENST00000370647.8:c.403T>A ENSP00000359681.4:p.Tyr135Asn
ENST00000370649.3:c.345+9577T>A ENSP00000359683.3:n.345+9577T>A
NM_001134670.1:c.403T>A NP_001128142.1:p.Tyr135Asn
NM_138413.3:c.892T>A NP_612422.2:p.Tyr298Asn
NM_138413.4:c.892T>A MANE Select NP_612422.2:p.Tyr298Asn
NM_001134670.2:c.403T>A NP_001128142.1:p.Tyr135Asn
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