Canonical Allele Identifier: CA5634165
Gene: HOGA1 HGNC NCBI

Linked Data

dbSNP Id: rs757059221
ExAC: 10:99359569 G / A
gnomAD v2: 10-99359569-G-A
gnomAD v3: 10-97599812-G-A
gnomAD v4: 10-97599812-G-A
COSMIC: COSM4598089
MyVariant Identifiers: chr10:g.99359569G>A (hg19) chr10:g.97599812G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97599812G>A , CM000672.2:g.97599812G>A GRCh38
NC_000010.10:g.99359569G>A , CM000672.1:g.99359569G>A GRCh37
NC_000010.9:g.99349559G>A NCBI36
NG_027922.1:g.20468G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.601G>A MANE Select ENSP00000359680.4:p.Asp201Asn
ENST00000370642.4:c.11G>A
ENST00000370646.8:c.601G>A ENSP00000359680.4:p.Asp201Asn
ENST00000370647.8:c.212-2045G>A ENSP00000359681.4:n.212-2045G>A
ENST00000370649.3:c.212-2045G>A ENSP00000359683.3:n.212-2045G>A
ENST00000465608.1:n.1445G>A
NM_001134670.1:c.212-2045G>A NP_001128142.1:n.212-2045G>A
NM_138413.3:c.601G>A NP_612422.2:p.Asp201Asn
NM_138413.4:c.601G>A MANE Select NP_612422.2:p.Asp201Asn
NM_001134670.2:c.212-2045G>A NP_001128142.1:n.212-2045G>A
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