Canonical Allele Identifier: CA5634176

Gene: HOGA1

Linked Data

• dbSNP Id: rs776660476
• ExAC: 10:99359786 C / CCTCA
• gnomAD v2: 10-99359786-C-CCTCA
• gnomAD v3: 10-97600029-C-CCTCA
• gnomAD v4: 10-97600029-C-CCTCA
• MyVariant Identifiers: chr10:g.99359786_99359787insCTCA (hg19) ; chr10:g.97600029_97600030insCTCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97600029_97600030insCTCA , CM000672.2:g.97600029_97600030insCTCA	GRCh38
NC_000010.10:g.99359786_99359787insCTCA , CM000672.1:g.99359786_99359787insCTCA	GRCh37
NC_000010.9:g.99349776_99349777insCTCA	NCBI36
NG_027922.1:g.20685_20686insCTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.604-38_604-37insCTCA MANE Select	ENSP00000359680.4:n.604-38_604-37insCTCA
ENST00000370642.4:c.14-38_14-37insCTCA
ENST00000370646.8:c.604-38_604-37insCTCA	ENSP00000359680.4:n.604-38_604-37insCTCA
ENST00000370647.8:c.212-1828_212-1827insCTCA	ENSP00000359681.4:n.212-1828_212-1827insCTCA
ENST00000370649.3:c.212-1828_212-1827insCTCA	ENSP00000359683.3:n.212-1828_212-1827insCTCA
ENST00000465608.1:n.1662_1663insCTCA
NM_001134670.1:c.212-1828_212-1827insCTCA	NP_001128142.1:n.212-1828_212-1827insCTCA
NM_138413.3:c.604-38_604-37insCTCA	NP_612422.2:n.604-38_604-37insCTCA
NM_138413.4:c.604-38_604-37insCTCA MANE Select	NP_612422.2:n.604-38_604-37insCTCA
NM_001134670.2:c.212-1828_212-1827insCTCA	NP_001128142.1:n.212-1828_212-1827insCTCA