Canonical Allele Identifier: CA471092779

Gene: HOGA1

Linked Data

• MyVariant Identifiers: chr10:g.99371335C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97611578C>G , CM000672.2:g.97611578C>G	GRCh38
NC_000010.10:g.99371335C>G , CM000672.1:g.99371335C>G	GRCh37
NC_000010.9:g.99361325C>G	NCBI36
NG_027922.1:g.32234C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.903C>G MANE Select	ENSP00000359680.4:p.Pro301=
ENST00000370646.8:c.903C>G	ENSP00000359680.4:p.Pro301=
ENST00000370647.8:c.414C>G	ENSP00000359681.4:p.Pro138=
ENST00000370649.3:c.345+9588C>G	ENSP00000359683.3:n.345+9588C>G
NM_001134670.1:c.414C>G	NP_001128142.1:p.Pro138=
NM_138413.3:c.903C>G	NP_612422.2:p.Pro301=
NM_138413.4:c.903C>G MANE Select	NP_612422.2:p.Pro301=
NM_001134670.2:c.414C>G	NP_001128142.1:p.Pro138=