Canonical Allele Identifier: CA377977093
Gene: HOGA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.99358636C>A (hg19) chr10:g.97598879C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97598879C>A , CM000672.2:g.97598879C>A GRCh38
NC_000010.10:g.99358636C>A , CM000672.1:g.99358636C>A GRCh37
NC_000010.9:g.99348626C>A NCBI36
NG_027922.1:g.19535C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.316C>A MANE Select ENSP00000359680.4:p.Leu106Met
ENST00000370646.8:c.316C>A ENSP00000359680.4:p.Leu106Met
ENST00000370647.8:c.212-2978C>A ENSP00000359681.4:n.212-2978C>A
ENST00000370649.3:c.212-2978C>A ENSP00000359683.3:n.212-2978C>A
ENST00000465608.1:n.697C>A
NM_001134670.1:c.212-2978C>A NP_001128142.1:n.212-2978C>A
NM_138413.3:c.316C>A NP_612422.2:p.Leu106Met
NM_138413.4:c.316C>A MANE Select NP_612422.2:p.Leu106Met
NM_001134670.2:c.212-2978C>A NP_001128142.1:n.212-2978C>A
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