Canonical Allele Identifier: CA915947524

Gene: HOGA1

Linked Data

• ClinVar Variation Id: 793282
• ClinVar RCV Id: RCV000976459
• dbSNP Id: rs1589907734

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97598911A>C , CM000672.2:g.97598911A>C	GRCh38
NC_000010.10:g.99358668A>C , CM000672.1:g.99358668A>C	GRCh37
NC_000010.9:g.99348658A>C	NCBI36
NG_027922.1:g.19567A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.340+8A>C MANE Select	ENSP00000359680.4:n.340+8A>C
ENST00000370646.8:c.340+8A>C	ENSP00000359680.4:n.340+8A>C
ENST00000370647.8:c.212-2946A>C	ENSP00000359681.4:n.212-2946A>C
ENST00000370649.3:c.212-2946A>C	ENSP00000359683.3:n.212-2946A>C
ENST00000465608.1:n.721+8A>C
NM_001134670.1:c.212-2946A>C	NP_001128142.1:n.212-2946A>C
NM_138413.3:c.340+8A>C	NP_612422.2:n.340+8A>C
NM_138413.4:c.340+8A>C MANE Select	NP_612422.2:n.340+8A>C
NM_001134670.2:c.212-2946A>C	NP_001128142.1:n.212-2946A>C