Canonical Allele Identifier: CA377979236

Gene: HOGA1

Linked Data

• MyVariant Identifiers: chr10:g.99359559C>G (hg19) ; chr10:g.97599802C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97599802C>G , CM000672.2:g.97599802C>G	GRCh38
NC_000010.10:g.99359559C>G , CM000672.1:g.99359559C>G	GRCh37
NC_000010.9:g.99349549C>G	NCBI36
NG_027922.1:g.20458C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.591C>G MANE Select	ENSP00000359680.4:p.Asp197Glu
ENST00000370642.4:c.1C>G
ENST00000370646.8:c.591C>G	ENSP00000359680.4:p.Asp197Glu
ENST00000370647.8:c.212-2055C>G	ENSP00000359681.4:n.212-2055C>G
ENST00000370649.3:c.212-2055C>G	ENSP00000359683.3:n.212-2055C>G
ENST00000465608.1:n.1435C>G
NM_001134670.1:c.212-2055C>G	NP_001128142.1:n.212-2055C>G
NM_138413.3:c.591C>G	NP_612422.2:p.Asp197Glu
NM_138413.4:c.591C>G MANE Select	NP_612422.2:p.Asp197Glu
NM_001134670.2:c.212-2055C>G	NP_001128142.1:n.212-2055C>G