Canonical Allele Identifier: CA377983607

Gene: HOGA1

Linked Data

• gnomAD v4: 10-97611594-C-T
• MyVariant Identifiers: chr10:g.99371351C>T (hg19) ; chr10:g.97611594C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97611594C>T , CM000672.2:g.97611594C>T	GRCh38
NC_000010.10:g.99371351C>T , CM000672.1:g.99371351C>T	GRCh37
NC_000010.9:g.99361341C>T	NCBI36
NG_027922.1:g.32250C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370646.9:c.919C>T MANE Select	ENSP00000359680.4:p.Gln307Ter
ENST00000370646.8:c.919C>T	ENSP00000359680.4:p.Gln307Ter
ENST00000370647.8:c.430C>T	ENSP00000359681.4:p.Gln144Ter
ENST00000370649.3:c.345+9604C>T	ENSP00000359683.3:n.345+9604C>T
NM_001134670.1:c.430C>T	NP_001128142.1:p.Gln144Ter
NM_138413.3:c.919C>T	NP_612422.2:p.Gln307Ter
NM_138413.4:c.919C>T MANE Select	NP_612422.2:p.Gln307Ter
NM_001134670.2:c.430C>T	NP_001128142.1:p.Gln144Ter