Canonical Allele Identifier: CA1977301018

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446028T= , CM000673.2:g.61446028T=	GRCh38
NC_000011.9:g.61213500T= , CM000673.1:g.61213500T=	GRCh37
NC_000011.8:g.60970076T=	NCBI36
NG_023393.1:g.20904T= , LRG_519:g.20904T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.458T= MANE Select	ENSP00000301761.3:p.Leu153=
ENST00000301761.6:c.458T=	ENSP00000301761.2:p.Leu153=
ENST00000536670.5:n.396+7915T=
ENST00000537782.5:c.*104T=	ENSP00000469951.1:n.*104T=
ENST00000538594.5:c.370+7915T=	ENSP00000440939.1:n.370+7915T=
ENST00000541135.5:c.377+7908T=	ENSP00000443130.1:n.377+7908T=
ENST00000542074.1:c.*37T=	ENSP00000469670.1:n.*37T=
ENST00000542794.5:c.*460T=	ENSP00000439983.1:n.*460T=
ENST00000543044.2:c.422T=	ENSP00000440219.1:p.Leu141=
ENST00000543265.1:c.*81T=	ENSP00000443660.1:n.*81T=
ENST00000544025.5:n.465+7915T=
ENST00000544801.5:c.370+7915T=	ENSP00000442581.1:n.370+7915T=
ENST00000544880.1:n.374+7915T=
NM_017841.2:c.458T= , LRG_519t1:c.458T=	NP_060311.1:p.Leu153=
NM_017841.4:c.458T= MANE Select	NP_060311.1:p.Leu153=