Canonical Allele Identifier: CA1930504968

Gene: HOGA1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97598926_97598928delinsCTG , CM000672.2:g.97598926_97598928delinsCTG	GRCh38
NC_000010.10:g.99358683_99358685delinsCTG , CM000672.1:g.99358683_99358685delinsCTG	GRCh37
NC_000010.9:g.99348673_99348675delinsCTG	NCBI36
NG_027922.1:g.19582_19584delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.340+23_340+25delinsCTG MANE Select	ENSP00000359680.4:n.340+23_340+25delinsCTG
ENST00000370646.8:c.340+23_340+25delinsCTG	ENSP00000359680.4:n.340+23_340+25delinsCTG
ENST00000370647.8:c.212-2931_212-2929delinsCTG	ENSP00000359681.4:n.212-2931_212-2929delinsCTG
ENST00000370649.3:c.212-2931_212-2929delinsCTG	ENSP00000359683.3:n.212-2931_212-2929delinsCTG
ENST00000465608.1:n.721+23_721+25delinsCTG
NM_001134670.1:c.212-2931_212-2929delinsCTG	NP_001128142.1:n.212-2931_212-2929delinsCTG
NM_138413.3:c.340+23_340+25delinsCTG	NP_612422.2:n.340+23_340+25delinsCTG
NM_138413.4:c.340+23_340+25delinsCTG MANE Select	NP_612422.2:n.340+23_340+25delinsCTG
NM_001134670.2:c.212-2931_212-2929delinsCTG	NP_001128142.1:n.212-2931_212-2929delinsCTG