Canonical Allele Identifier: CA377979401

Gene: HOGA1

Linked Data

• MyVariant Identifiers: chr10:g.99359825T>G (hg19) ; chr10:g.97600068T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97600068T>G , CM000672.2:g.97600068T>G	GRCh38
NC_000010.10:g.99359825T>G , CM000672.1:g.99359825T>G	GRCh37
NC_000010.9:g.99349815T>G	NCBI36
NG_027922.1:g.20724T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.605T>G MANE Select	ENSP00000359680.4:p.Val202Gly
ENST00000370642.4:c.15T>G
ENST00000370646.8:c.605T>G	ENSP00000359680.4:p.Val202Gly
ENST00000370647.8:c.212-1789T>G	ENSP00000359681.4:n.212-1789T>G
ENST00000370649.3:c.212-1789T>G	ENSP00000359683.3:n.212-1789T>G
ENST00000465608.1:n.1701T>G
NM_001134670.1:c.212-1789T>G	NP_001128142.1:n.212-1789T>G
NM_138413.3:c.605T>G	NP_612422.2:p.Val202Gly
NM_138413.4:c.605T>G MANE Select	NP_612422.2:p.Val202Gly
NM_001134670.2:c.212-1789T>G	NP_001128142.1:n.212-1789T>G