Canonical Allele Identifier: CA212683016

Gene: HOGA1

Linked Data

• dbSNP Id: rs1010321424
• gnomAD v2: 10-99371146-C-CAGTT
• gnomAD v3: 10-97611389-C-CAGTT
• gnomAD v4: 10-97611389-C-CAGTT
• MyVariant Identifiers: chr10:g.99371146_99371147insAGTT (hg19) ; chr10:g.97611389_97611390insAGTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97611391_97611394dup , CM000672.2:g.97611391_97611394dup	GRCh38
NC_000010.10:g.99371148_99371151dup , CM000672.1:g.99371148_99371151dup	GRCh37
NC_000010.9:g.99361138_99361141dup	NCBI36
NG_027922.1:g.32047_32050dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.835-119_835-116dup MANE Select	ENSP00000359680.4:n.835-119_835-116dup
ENST00000370646.8:c.835-119_835-116dup	ENSP00000359680.4:n.835-119_835-116dup
ENST00000370647.8:c.346-119_346-116dup	ENSP00000359681.4:n.346-119_346-116dup
ENST00000370649.3:c.345+9401_345+9404dup	ENSP00000359683.3:n.345+9401_345+9404dup
NM_001134670.1:c.346-119_346-116dup	NP_001128142.1:n.346-119_346-116dup
NM_138413.3:c.835-119_835-116dup	NP_612422.2:n.835-119_835-116dup
NM_138413.4:c.835-119_835-116dup MANE Select	NP_612422.2:n.835-119_835-116dup
NM_001134670.2:c.346-119_346-116dup	NP_001128142.1:n.346-119_346-116dup