Canonical Allele Identifier: CA595408301

Gene: HOGA1

Linked Data

• dbSNP Id: rs1281933590
• gnomAD v2: 10-99359671-G-C
• gnomAD v3: 10-97599914-G-C
• gnomAD v4: 10-97599914-G-C
• MyVariant Identifiers: chr10:g.99359671G>C (hg19) ; chr10:g.97599914G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97599914G>C , CM000672.2:g.97599914G>C	GRCh38
NC_000010.10:g.99359671G>C , CM000672.1:g.99359671G>C	GRCh37
NC_000010.9:g.99349661G>C	NCBI36
NG_027922.1:g.20570G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.603+100G>C MANE Select	ENSP00000359680.4:n.603+100G>C
ENST00000370642.4:c.13+100G>C
ENST00000370646.8:c.603+100G>C	ENSP00000359680.4:n.603+100G>C
ENST00000370647.8:c.212-1943G>C	ENSP00000359681.4:n.212-1943G>C
ENST00000370649.3:c.212-1943G>C	ENSP00000359683.3:n.212-1943G>C
ENST00000465608.1:n.1547G>C
NM_001134670.1:c.212-1943G>C	NP_001128142.1:n.212-1943G>C
NM_138413.3:c.603+100G>C	NP_612422.2:n.603+100G>C
NM_138413.4:c.603+100G>C MANE Select	NP_612422.2:n.603+100G>C
NM_001134670.2:c.212-1943G>C	NP_001128142.1:n.212-1943G>C