Canonical Allele Identifier: CA2739275970

Gene: HOGA1

Linked Data

• ClinVar Variation Id: 2856048
• ClinVar RCV Id: RCV003701713

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97600048A>T , CM000672.2:g.97600048A>T	GRCh38
NC_000010.10:g.99359805A>T , CM000672.1:g.99359805A>T	GRCh37
NC_000010.9:g.99349795A>T	NCBI36
NG_027922.1:g.20704A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.604-19A>T MANE Select	ENSP00000359680.4:n.604-19A>T
ENST00000370642.4:c.14-19A>T
ENST00000370646.8:c.604-19A>T	ENSP00000359680.4:n.604-19A>T
ENST00000370647.8:c.212-1809A>T	ENSP00000359681.4:n.212-1809A>T
ENST00000370649.3:c.212-1809A>T	ENSP00000359683.3:n.212-1809A>T
ENST00000465608.1:n.1681A>T
NM_001134670.1:c.212-1809A>T	NP_001128142.1:n.212-1809A>T
NM_138413.3:c.604-19A>T	NP_612422.2:n.604-19A>T
NM_138413.4:c.604-19A>T MANE Select	NP_612422.2:n.604-19A>T
NM_001134670.2:c.212-1809A>T	NP_001128142.1:n.212-1809A>T