Canonical Allele Identifier: CA471092073

Gene: HOGA1

Linked Data

• MyVariant Identifiers: chr10:g.99359835T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97600078T>A , CM000672.2:g.97600078T>A	GRCh38
NC_000010.10:g.99359835T>A , CM000672.1:g.99359835T>A	GRCh37
NC_000010.9:g.99349825T>A	NCBI36
NG_027922.1:g.20734T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.615T>A MANE Select	ENSP00000359680.4:p.Ile205=
ENST00000370642.4:c.25T>A
ENST00000370646.8:c.615T>A	ENSP00000359680.4:p.Ile205=
ENST00000370647.8:c.212-1779T>A	ENSP00000359681.4:n.212-1779T>A
ENST00000370649.3:c.212-1779T>A	ENSP00000359683.3:n.212-1779T>A
ENST00000465608.1:n.1711T>A
NM_001134670.1:c.212-1779T>A	NP_001128142.1:n.212-1779T>A
NM_138413.3:c.615T>A	NP_612422.2:p.Ile205=
NM_138413.4:c.615T>A MANE Select	NP_612422.2:p.Ile205=
NM_001134670.2:c.212-1779T>A	NP_001128142.1:n.212-1779T>A