Canonical Allele Identifier: CA2610411158

Gene: HOGA1

Linked Data

• gnomAD v4: 10-97600196-G-GTATCTCT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97600197_97600198insATCTCTT , CM000672.2:g.97600197_97600198insATCTCTT	GRCh38
NC_000010.10:g.99359954_99359955insATCTCTT , CM000672.1:g.99359954_99359955insATCTCTT	GRCh37
NC_000010.9:g.99349944_99349945insATCTCTT	NCBI36
NG_027922.1:g.20853_20854insATCTCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000370646.9:c.700+34_700+35insATCTCTT MANE Select	ENSP00000359680.4:n.700+34_700+35insATCTC...
ENST00000370642.4:c.110+34_110+35insATCTCTT
ENST00000370646.8:c.700+34_700+35insATCTCTT	ENSP00000359680.4:n.700+34_700+35insATCTC...
ENST00000370647.8:c.212-1660_212-1659insATCTCTT	ENSP00000359681.4:n.212-1660_212-1659insA...
ENST00000370649.3:c.212-1660_212-1659insATCTCTT	ENSP00000359683.3:n.212-1660_212-1659insA...
ENST00000465608.1:n.1830_1831insATCTCTT
NM_001134670.1:c.212-1660_212-1659insATCTCTT	NP_001128142.1:n.212-1660_212-1659insATCT...
NM_138413.3:c.700+34_700+35insATCTCTT	NP_612422.2:n.700+34_700+35insATCTCTT
NM_138413.4:c.700+34_700+35insATCTCTT MANE Select	NP_612422.2:n.700+34_700+35insATCTCTT
NM_001134670.2:c.212-1660_212-1659insATCTCTT	NP_001128142.1:n.212-1660_212-1659insATCT...