Canonical Allele Identifier: CA471092788

Gene: HOGA1

Linked Data

• dbSNP Id: rs2041196365
• MyVariant Identifiers: chr10:g.99371347C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97611590C>T , CM000672.2:g.97611590C>T	GRCh38
NC_000010.10:g.99371347C>T , CM000672.1:g.99371347C>T	GRCh37
NC_000010.9:g.99361337C>T	NCBI36
NG_027922.1:g.32246C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370646.9:c.915C>T MANE Select	ENSP00000359680.4:p.Pro305=
ENST00000370646.8:c.915C>T	ENSP00000359680.4:p.Pro305=
ENST00000370647.8:c.426C>T	ENSP00000359681.4:p.Pro142=
ENST00000370649.3:c.345+9600C>T	ENSP00000359683.3:n.345+9600C>T
NM_001134670.1:c.426C>T	NP_001128142.1:p.Pro142=
NM_138413.3:c.915C>T	NP_612422.2:p.Pro305=
NM_138413.4:c.915C>T MANE Select	NP_612422.2:p.Pro305=
NM_001134670.2:c.426C>T	NP_001128142.1:p.Pro142=