Canonical Allele Identifier: CA1930506758
Gene: HOGA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97611161T= , CM000672.2:g.97611161T= GRCh38
NC_000010.10:g.99370918T= , CM000672.1:g.99370918T= GRCh37
NC_000010.9:g.99360908T= NCBI36
NG_027922.1:g.31817T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.835-349T= MANE Select ENSP00000359680.4:n.835-349T=
ENST00000370646.8:c.835-349T= ENSP00000359680.4:n.835-349T=
ENST00000370647.8:c.346-349T= ENSP00000359681.4:n.346-349T=
ENST00000370649.3:c.345+9171T= ENSP00000359683.3:n.345+9171T=
NM_001134670.1:c.346-349T= NP_001128142.1:n.346-349T=
NM_138413.3:c.835-349T= NP_612422.2:n.835-349T=
NM_138413.4:c.835-349T= MANE Select NP_612422.2:n.835-349T=
NM_001134670.2:c.346-349T= NP_001128142.1:n.346-349T=
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