Canonical Allele Identifier: CA1977301059

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446039G= , CM000673.2:g.61446039G=	GRCh38
NC_000011.9:g.61213511G= , CM000673.1:g.61213511G=	GRCh37
NC_000011.8:g.60970087G=	NCBI36
NG_023393.1:g.20915G= , LRG_519:g.20915G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.469G= MANE Select	ENSP00000301761.3:p.Asp157=
ENST00000301761.6:c.469G=	ENSP00000301761.2:p.Asp157=
ENST00000536670.5:n.396+7926G=
ENST00000537782.5:c.*115G=	ENSP00000469951.1:n.*115G=
ENST00000538594.5:c.370+7926G=	ENSP00000440939.1:n.370+7926G=
ENST00000541135.5:c.377+7919G=	ENSP00000443130.1:n.377+7919G=
ENST00000542074.1:c.*48G=	ENSP00000469670.1:n.*48G=
ENST00000542794.5:c.*471G=	ENSP00000439983.1:n.*471G=
ENST00000543044.2:c.433G=	ENSP00000440219.1:p.Asp145=
ENST00000543265.1:c.*92G=	ENSP00000443660.1:n.*92G=
ENST00000544025.5:n.465+7926G=
ENST00000544801.5:c.370+7926G=	ENSP00000442581.1:n.370+7926G=
ENST00000544880.1:n.374+7926G=
NM_017841.2:c.469G= , LRG_519t1:c.469G=	NP_060311.1:p.Asp157=
NM_017841.4:c.469G= MANE Select	NP_060311.1:p.Asp157=