Canonical Allele Identifier: CA1977301008

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446027C= , CM000673.2:g.61446027C=	GRCh38
NC_000011.9:g.61213499C= , CM000673.1:g.61213499C=	GRCh37
NC_000011.8:g.60970075C=	NCBI36
NG_023393.1:g.20903C= , LRG_519:g.20903C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.457C= MANE Select	ENSP00000301761.3:p.Leu153=
ENST00000301761.6:c.457C=	ENSP00000301761.2:p.Leu153=
ENST00000536670.5:n.396+7914C=
ENST00000537782.5:c.*103C=	ENSP00000469951.1:n.*103C=
ENST00000538594.5:c.370+7914C=	ENSP00000440939.1:n.370+7914C=
ENST00000541135.5:c.377+7907C=	ENSP00000443130.1:n.377+7907C=
ENST00000542074.1:c.*36C=	ENSP00000469670.1:n.*36C=
ENST00000542794.5:c.*459C=	ENSP00000439983.1:n.*459C=
ENST00000543044.2:c.421C=	ENSP00000440219.1:p.Leu141=
ENST00000543265.1:c.*80C=	ENSP00000443660.1:n.*80C=
ENST00000544025.5:n.465+7914C=
ENST00000544801.5:c.370+7914C=	ENSP00000442581.1:n.370+7914C=
ENST00000544880.1:n.374+7914C=
NM_017841.2:c.457C= , LRG_519t1:c.457C=	NP_060311.1:p.Leu153=
NM_017841.4:c.457C= MANE Select	NP_060311.1:p.Leu153=