Canonical Allele Identifier: CA2789141570
Gene: HOGA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97598892_97598893insTCGCAGGCAGATGTCTG , CM000672.2:g.97598892_97598893insTCGCAGGCAGATGTCTG GRCh38
NC_000010.10:g.99358649_99358650insTCGCAGGCAGATGTCTG , CM000672.1:g.99358649_99358650insTCGCAGGCAGATGTCTG GRCh37
NC_000010.9:g.99348639_99348640insTCGCAGGCAGATGTCTG NCBI36
NG_027922.1:g.19548_19549insTCGCAGGCAGATGTCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.329_330insTCGCAGGCAGATGTCTG MANE Select ENSP00000359680.4:p.Gly111ArgfsTer17
ENST00000370646.8:c.329_330insTCGCAGGCAGATGTCTG ENSP00000359680.4:p.Gly111ArgfsTer17
ENST00000370647.8:c.212-2965_212-2964insTCGCAGGCAGATGTCTG ENSP00000359681.4:n.212-2965_212-2964insTCGCAGGCAGATGTCTG
ENST00000370649.3:c.212-2965_212-2964insTCGCAGGCAGATGTCTG ENSP00000359683.3:n.212-2965_212-2964insTCGCAGGCAGATGTCTG
ENST00000465608.1:n.710_711insTCGCAGGCAGATGTCTG
NM_001134670.1:c.212-2965_212-2964insTCGCAGGCAGATGTCTG NP_001128142.1:n.212-2965_212-2964insTCGCAGGCAGATGTCTG
NM_138413.3:c.329_330insTCGCAGGCAGATGTCTG NP_612422.2:p.Gly111ArgfsTer17
NM_138413.4:c.329_330insTCGCAGGCAGATGTCTG MANE Select NP_612422.2:p.Gly111ArgfsTer17
NM_001134670.2:c.212-2965_212-2964insTCGCAGGCAGATGTCTG NP_001128142.1:n.212-2965_212-2964insTCGCAGGCAGATGTCTG