Canonical Allele Identifier: CA377979398

Gene: HOGA1

Linked Data

• gnomAD v4: 10-97600067-G-T
• MyVariant Identifiers: chr10:g.99359824G>T (hg19) ; chr10:g.97600067G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97600067G>T , CM000672.2:g.97600067G>T	GRCh38
NC_000010.10:g.99359824G>T , CM000672.1:g.99359824G>T	GRCh37
NC_000010.9:g.99349814G>T	NCBI36
NG_027922.1:g.20723G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.604G>T MANE Select	ENSP00000359680.4:p.Val202Leu
ENST00000370642.4:c.14G>T
ENST00000370646.8:c.604G>T	ENSP00000359680.4:p.Val202Leu
ENST00000370647.8:c.212-1790G>T	ENSP00000359681.4:n.212-1790G>T
ENST00000370649.3:c.212-1790G>T	ENSP00000359683.3:n.212-1790G>T
ENST00000465608.1:n.1700G>T
NM_001134670.1:c.212-1790G>T	NP_001128142.1:n.212-1790G>T
NM_138413.3:c.604G>T	NP_612422.2:p.Val202Leu
NM_138413.4:c.604G>T MANE Select	NP_612422.2:p.Val202Leu
NM_001134670.2:c.212-1790G>T	NP_001128142.1:n.212-1790G>T