Canonical Allele Identifier: CA5634309
Gene: HOGA1 HGNC NCBI

Linked Data

dbSNP Id: rs757466556
ExAC: 10:99371343 C / T
gnomAD v2: 10-99371343-C-T
gnomAD v4: 10-97611586-C-T
MyVariant Identifiers: chr10:g.99371343C>T (hg19) chr10:g.97611586C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97611586C>T , CM000672.2:g.97611586C>T GRCh38
NC_000010.10:g.99371343C>T , CM000672.1:g.99371343C>T GRCh37
NC_000010.9:g.99361333C>T NCBI36
NG_027922.1:g.32242C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370646.9:c.911C>T MANE Select ENSP00000359680.4:p.Ala304Val
ENST00000370646.8:c.911C>T ENSP00000359680.4:p.Ala304Val
ENST00000370647.8:c.422C>T ENSP00000359681.4:p.Ala141Val
ENST00000370649.3:c.345+9596C>T ENSP00000359683.3:n.345+9596C>T
NM_001134670.1:c.422C>T NP_001128142.1:p.Ala141Val
NM_138413.3:c.911C>T NP_612422.2:p.Ala304Val
NM_138413.4:c.911C>T MANE Select NP_612422.2:p.Ala304Val
NM_001134670.2:c.422C>T NP_001128142.1:p.Ala141Val
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