Canonical Allele Identifier: CA1977301082

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446047G= , CM000673.2:g.61446047G=	GRCh38
NC_000011.9:g.61213519G= , CM000673.1:g.61213519G=	GRCh37
NC_000011.8:g.60970095G=	NCBI36
NG_023393.1:g.20923G= , LRG_519:g.20923G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.477G= MANE Select	ENSP00000301761.3:p.Glu159=
ENST00000301761.6:c.477G=	ENSP00000301761.2:p.Glu159=
ENST00000536670.5:n.396+7934G=
ENST00000537782.5:c.*123G=	ENSP00000469951.1:n.*123G=
ENST00000538594.5:c.370+7934G=	ENSP00000440939.1:n.370+7934G=
ENST00000541135.5:c.377+7927G=	ENSP00000443130.1:n.377+7927G=
ENST00000542074.1:c.*56G=	ENSP00000469670.1:n.*56G=
ENST00000542794.5:c.*479G=	ENSP00000439983.1:n.*479G=
ENST00000543044.2:c.441G=	ENSP00000440219.1:p.Glu147=
ENST00000543265.1:c.*100G=	ENSP00000443660.1:n.*100G=
ENST00000544025.5:n.465+7934G=
ENST00000544801.5:c.370+7934G=	ENSP00000442581.1:n.370+7934G=
ENST00000544880.1:n.374+7934G=
NM_017841.2:c.477G= , LRG_519t1:c.477G=	NP_060311.1:p.Glu159=
NM_017841.4:c.477G= MANE Select	NP_060311.1:p.Glu159=