Canonical Allele Identifier: CA2697558724

Gene: HOGA1

Linked Data

• ClinVar Variation Id: 2743992
• ClinVar RCV Id: RCV003560624

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97598910C>T , CM000672.2:g.97598910C>T	GRCh38
NC_000010.10:g.99358667C>T , CM000672.1:g.99358667C>T	GRCh37
NC_000010.9:g.99348657C>T	NCBI36
NG_027922.1:g.19566C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370646.9:c.340+7C>T MANE Select	ENSP00000359680.4:n.340+7C>T
ENST00000370646.8:c.340+7C>T	ENSP00000359680.4:n.340+7C>T
ENST00000370647.8:c.212-2947C>T	ENSP00000359681.4:n.212-2947C>T
ENST00000370649.3:c.212-2947C>T	ENSP00000359683.3:n.212-2947C>T
ENST00000465608.1:n.721+7C>T
NM_001134670.1:c.212-2947C>T	NP_001128142.1:n.212-2947C>T
NM_138413.3:c.340+7C>T	NP_612422.2:n.340+7C>T
NM_138413.4:c.340+7C>T MANE Select	NP_612422.2:n.340+7C>T
NM_001134670.2:c.212-2947C>T	NP_001128142.1:n.212-2947C>T