Canonical Allele Identifier: CA377979299

Gene: HOGA1

Linked Data

• dbSNP Id: rs1187782084
• MyVariant Identifiers: chr10:g.99359570A>T (hg19) ; chr10:g.97599813A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97599813A>T , CM000672.2:g.97599813A>T	GRCh38
NC_000010.10:g.99359570A>T , CM000672.1:g.99359570A>T	GRCh37
NC_000010.9:g.99349560A>T	NCBI36
NG_027922.1:g.20469A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.602A>T MANE Select	ENSP00000359680.4:p.Asp201Val
ENST00000370642.4:c.12A>T
ENST00000370646.8:c.602A>T	ENSP00000359680.4:p.Asp201Val
ENST00000370647.8:c.212-2044A>T	ENSP00000359681.4:n.212-2044A>T
ENST00000370649.3:c.212-2044A>T	ENSP00000359683.3:n.212-2044A>T
ENST00000465608.1:n.1446A>T
NM_001134670.1:c.212-2044A>T	NP_001128142.1:n.212-2044A>T
NM_138413.3:c.602A>T	NP_612422.2:p.Asp201Val
NM_138413.4:c.602A>T MANE Select	NP_612422.2:p.Asp201Val
NM_001134670.2:c.212-2044A>T	NP_001128142.1:n.212-2044A>T