Canonical Allele Identifier: CA5634201

Gene: HOGA1

Linked Data

• dbSNP Id: rs775016553
• ExAC: 10:99359949 ATGGGTGACC / A
• gnomAD v2: 10-99359949-ATGGGTGACC-A
• gnomAD v4: 10-97600192-ATGGGTGACC-A
• MyVariant Identifiers: chr10:g.99359950_99359958del (hg19) ; chr10:g.97600193_97600201del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97600193_97600201del , CM000672.2:g.97600193_97600201del	GRCh38
NC_000010.10:g.99359950_99359958del , CM000672.1:g.99359950_99359958del	GRCh37
NC_000010.9:g.99349940_99349948del	NCBI36
NG_027922.1:g.20849_20857del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370646.9:c.700+30_700+38del MANE Select	ENSP00000359680.4:n.700+30_700+38del
ENST00000370642.4:c.110+30_110+38del
ENST00000370646.8:c.700+30_700+38del	ENSP00000359680.4:n.700+30_700+38del
ENST00000370647.8:c.212-1664_212-1656del	ENSP00000359681.4:n.212-1664_212-1656del
ENST00000370649.3:c.212-1664_212-1656del	ENSP00000359683.3:n.212-1664_212-1656del
ENST00000465608.1:n.1826_1834del
NM_001134670.1:c.212-1664_212-1656del	NP_001128142.1:n.212-1664_212-1656del
NM_138413.3:c.700+30_700+38del	NP_612422.2:n.700+30_700+38del
NM_138413.4:c.700+30_700+38del MANE Select	NP_612422.2:n.700+30_700+38del
NM_001134670.2:c.212-1664_212-1656del	NP_001128142.1:n.212-1664_212-1656del