Canonical Allele Identifier: CA1977301091

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446056T= , CM000673.2:g.61446056T=	GRCh38
NC_000011.9:g.61213528T= , CM000673.1:g.61213528T=	GRCh37
NC_000011.8:g.60970104T=	NCBI36
NG_023393.1:g.20932T= , LRG_519:g.20932T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.486T= MANE Select	ENSP00000301761.3:p.Phe162=
ENST00000301761.6:c.486T=	ENSP00000301761.2:p.Phe162=
ENST00000536670.5:n.396+7943T=
ENST00000537782.5:c.*132T=	ENSP00000469951.1:n.*132T=
ENST00000538594.5:c.370+7943T=	ENSP00000440939.1:n.370+7943T=
ENST00000541135.5:c.377+7936T=	ENSP00000443130.1:n.377+7936T=
ENST00000542074.1:c.*65T=	ENSP00000469670.1:n.*65T=
ENST00000542794.5:c.*488T=	ENSP00000439983.1:n.*488T=
ENST00000543044.2:c.450T=	ENSP00000440219.1:p.Phe150=
ENST00000543265.1:c.*109T=	ENSP00000443660.1:n.*109T=
ENST00000544025.5:n.465+7943T=
ENST00000544801.5:c.370+7943T=	ENSP00000442581.1:n.370+7943T=
ENST00000544880.1:n.374+7943T=
NM_017841.2:c.486T= , LRG_519t1:c.486T=	NP_060311.1:p.Phe162=
NM_017841.4:c.486T= MANE Select	NP_060311.1:p.Phe162=