Canonical Allele Identifier: CA471092740
Gene: HOGA1 HGNC NCBI

Linked Data

dbSNP Id: rs1444436917
gnomAD v2: 10-99371296-G-C
gnomAD v3: 10-97611539-G-C
gnomAD v4: 10-97611539-G-C
MyVariant Identifiers: chr10:g.99371296G>C (hg19) chr10:g.97611539G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97611539G>C , CM000672.2:g.97611539G>C GRCh38
NC_000010.10:g.99371296G>C , CM000672.1:g.99371296G>C GRCh37
NC_000010.9:g.99361286G>C NCBI36
NG_027922.1:g.32195G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.864G>C MANE Select ENSP00000359680.4:p.Leu288=
ENST00000370646.8:c.864G>C ENSP00000359680.4:p.Leu288=
ENST00000370647.8:c.375G>C ENSP00000359681.4:p.Leu125=
ENST00000370649.3:c.345+9549G>C ENSP00000359683.3:n.345+9549G>C
NM_001134670.1:c.375G>C NP_001128142.1:p.Leu125=
NM_138413.3:c.864G>C NP_612422.2:p.Leu288=
NM_138413.4:c.864G>C MANE Select NP_612422.2:p.Leu288=
NM_001134670.2:c.375G>C NP_001128142.1:p.Leu125=
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