Canonical Allele Identifier: CA471092833

Gene: HOGA1

Linked Data

• MyVariant Identifiers: chr10:g.99371392T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97611635T>C , CM000672.2:g.97611635T>C	GRCh38
NC_000010.10:g.99371392T>C , CM000672.1:g.99371392T>C	GRCh37
NC_000010.9:g.99361382T>C	NCBI36
NG_027922.1:g.32291T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.960T>C MANE Select	ENSP00000359680.4:p.Asp320=
ENST00000370646.8:c.960T>C	ENSP00000359680.4:p.Asp320=
ENST00000370647.8:c.471T>C	ENSP00000359681.4:p.Asp157=
ENST00000370649.3:c.345+9645T>C	ENSP00000359683.3:n.345+9645T>C
NM_001134670.1:c.471T>C	NP_001128142.1:p.Asp157=
NM_138413.3:c.960T>C	NP_612422.2:p.Asp320=
NM_138413.4:c.960T>C MANE Select	NP_612422.2:p.Asp320=
NM_001134670.2:c.471T>C	NP_001128142.1:p.Asp157=