Canonical Allele Identifier: CA380685492

Gene: SDHAF2

Linked Data

• MyVariant Identifiers: chr11:g.61213508C>A (hg19) ; chr11:g.61446036C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446036C>A , CM000673.2:g.61446036C>A	GRCh38
NC_000011.9:g.61213508C>A , CM000673.1:g.61213508C>A	GRCh37
NC_000011.8:g.60970084C>A	NCBI36
NG_023393.1:g.20912C>A , LRG_519:g.20912C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.466C>A MANE Select	ENSP00000301761.3:p.Pro156Thr
ENST00000301761.6:c.466C>A	ENSP00000301761.2:p.Pro156Thr
ENST00000536670.5:n.396+7923C>A
ENST00000537782.5:c.*112C>A	ENSP00000469951.1:n.*112C>A
ENST00000538594.5:c.370+7923C>A	ENSP00000440939.1:n.370+7923C>A
ENST00000541135.5:c.377+7916C>A	ENSP00000443130.1:n.377+7916C>A
ENST00000542074.1:c.*45C>A	ENSP00000469670.1:n.*45C>A
ENST00000542794.5:c.*468C>A	ENSP00000439983.1:n.*468C>A
ENST00000543044.2:c.430C>A	ENSP00000440219.1:p.Pro144Thr
ENST00000543265.1:c.*89C>A	ENSP00000443660.1:n.*89C>A
ENST00000544025.5:n.465+7923C>A
ENST00000544801.5:c.370+7923C>A	ENSP00000442581.1:n.370+7923C>A
ENST00000544880.1:n.374+7923C>A
NM_017841.2:c.466C>A , LRG_519t1:c.466C>A	NP_060311.1:p.Pro156Thr
NM_017841.4:c.466C>A MANE Select	NP_060311.1:p.Pro156Thr