Canonical Allele Identifier: CA377983559
Gene: HOGA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.99371342G>C (hg19) chr10:g.97611585G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97611585G>C , CM000672.2:g.97611585G>C GRCh38
NC_000010.10:g.99371342G>C , CM000672.1:g.99371342G>C GRCh37
NC_000010.9:g.99361332G>C NCBI36
NG_027922.1:g.32241G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370646.9:c.910G>C MANE Select ENSP00000359680.4:p.Ala304Pro
ENST00000370646.8:c.910G>C ENSP00000359680.4:p.Ala304Pro
ENST00000370647.8:c.421G>C ENSP00000359681.4:p.Ala141Pro
ENST00000370649.3:c.345+9595G>C ENSP00000359683.3:n.345+9595G>C
NM_001134670.1:c.421G>C NP_001128142.1:p.Ala141Pro
NM_138413.3:c.910G>C NP_612422.2:p.Ala304Pro
NM_138413.4:c.910G>C MANE Select NP_612422.2:p.Ala304Pro
NM_001134670.2:c.421G>C NP_001128142.1:p.Ala141Pro
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