Canonical Allele Identifier: CA377979216
Gene: HOGA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.99359555A>C (hg19) chr10:g.97599798A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97599798A>C , CM000672.2:g.97599798A>C GRCh38
NC_000010.10:g.99359555A>C , CM000672.1:g.99359555A>C GRCh37
NC_000010.9:g.99349545A>C NCBI36
NG_027922.1:g.20454A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.587A>C MANE Select ENSP00000359680.4:p.Lys196Thr
ENST00000370646.8:c.587A>C ENSP00000359680.4:p.Lys196Thr
ENST00000370647.8:c.212-2059A>C ENSP00000359681.4:n.212-2059A>C
ENST00000370649.3:c.212-2059A>C ENSP00000359683.3:n.212-2059A>C
ENST00000465608.1:n.1431A>C
NM_001134670.1:c.212-2059A>C NP_001128142.1:n.212-2059A>C
NM_138413.3:c.587A>C NP_612422.2:p.Lys196Thr
NM_138413.4:c.587A>C MANE Select NP_612422.2:p.Lys196Thr
NM_001134670.2:c.212-2059A>C NP_001128142.1:n.212-2059A>C
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