Canonical Allele Identifier: CA380684157

Gene: SDHAF2

Linked Data

• ClinVar Variation Id: 2706257
• ClinVar RCV Id: RCV003518081
• dbSNP Id: rs1862016537
• MyVariant Identifiers: chr11:g.61205541T>C (hg19) ; chr11:g.61438069T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61438069T>C , CM000673.2:g.61438069T>C	GRCh38
NC_000011.9:g.61205541T>C , CM000673.1:g.61205541T>C	GRCh37
NC_000011.8:g.60962117T>C	NCBI36
NG_023393.1:g.12945T>C , LRG_519:g.12945T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.326T>C MANE Select	ENSP00000301761.3:p.Ile109Thr
ENST00000301761.6:c.326T>C	ENSP00000301761.2:p.Ile109Thr
ENST00000359614.9:c.326T>C	ENSP00000352630.5:p.Ile109Thr
ENST00000534878.5:c.326T>C	ENSP00000471030.1:p.Ile109Thr
ENST00000536250.1:c.*328T>C	ENSP00000471120.1:n.*328T>C
ENST00000536670.5:n.352T>C
ENST00000537782.5:c.326T>C	ENSP00000469951.1:p.Ile109Thr
ENST00000538594.5:c.326T>C	ENSP00000440939.1:p.Ile109Thr
ENST00000541135.5:c.326T>C	ENSP00000443130.1:p.Ile109Thr
ENST00000542074.1:c.37-7872T>C	ENSP00000469670.1:n.37-7872T>C
ENST00000542794.5:c.*328T>C	ENSP00000439983.1:n.*328T>C
ENST00000543044.2:c.290T>C	ENSP00000440219.1:p.Ile97Thr
ENST00000543265.1:c.260+221T>C	ENSP00000443660.1:n.260+221T>C
ENST00000544025.5:n.421T>C
ENST00000544801.5:c.326T>C	ENSP00000442581.1:p.Ile109Thr
ENST00000544880.1:n.330T>C
NM_017841.2:c.326T>C , LRG_519t1:c.326T>C	NP_060311.1:p.Ile109Thr
NM_017841.4:c.326T>C MANE Select	NP_060311.1:p.Ile109Thr