Canonical Allele Identifier: CA1977300972

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446014_61446016delinsCAA , CM000673.2:g.61446014_61446016delinsCAA	GRCh38
NC_000011.9:g.61213486_61213488delinsCAA , CM000673.1:g.61213486_61213488delinsCAA	GRCh37
NC_000011.8:g.60970062_60970064delinsCAA	NCBI36
NG_023393.1:g.20890_20892delinsCAA , LRG_519:g.20890_20892delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.444_446delinsCAA MANE Select	ENSP00000301761.3:p.Asn148=
ENST00000301761.6:c.444_446delinsCAA	ENSP00000301761.2:p.Asn148=
ENST00000536670.5:n.396+7901_396+7903delinsCAA
ENST00000537782.5:c.*90_*92delinsCAA	ENSP00000469951.1:n.*90_*92delinsCAA
ENST00000538594.5:c.370+7901_370+7903delinsCAA	ENSP00000440939.1:n.370+7901_370+7903delinsCAA
ENST00000541135.5:c.377+7894_377+7896delinsCAA	ENSP00000443130.1:n.377+7894_377+7896delinsCAA
ENST00000542074.1:c.*23_*25delinsCAA	ENSP00000469670.1:n.*23_*25delinsCAA
ENST00000542794.5:c.*446_*448delinsCAA	ENSP00000439983.1:n.*446_*448delinsCAA
ENST00000543044.2:c.408_410delinsCAA	ENSP00000440219.1:p.Asn136=
ENST00000543265.1:c.*67_*69delinsCAA	ENSP00000443660.1:n.*67_*69delinsCAA
ENST00000544025.5:n.465+7901_465+7903delinsCAA
ENST00000544801.5:c.370+7901_370+7903delinsCAA	ENSP00000442581.1:n.370+7901_370+7903delinsCAA
ENST00000544880.1:n.374+7901_374+7903delinsCAA
NM_017841.2:c.444_446delinsCAA , LRG_519t1:c.444_446delinsCAA	NP_060311.1:p.Asn148=
NM_017841.4:c.444_446delinsCAA MANE Select	NP_060311.1:p.Asn148=