Canonical Allele Identifier: CA1977300995

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446021C= , CM000673.2:g.61446021C=	GRCh38
NC_000011.9:g.61213493C= , CM000673.1:g.61213493C=	GRCh37
NC_000011.8:g.60970069C=	NCBI36
NG_023393.1:g.20897C= , LRG_519:g.20897C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.451C= MANE Select	ENSP00000301761.3:p.Gln151=
ENST00000301761.6:c.451C=	ENSP00000301761.2:p.Gln151=
ENST00000536670.5:n.396+7908C=
ENST00000537782.5:c.*97C=	ENSP00000469951.1:n.*97C=
ENST00000538594.5:c.370+7908C=	ENSP00000440939.1:n.370+7908C=
ENST00000541135.5:c.377+7901C=	ENSP00000443130.1:n.377+7901C=
ENST00000542074.1:c.*30C=	ENSP00000469670.1:n.*30C=
ENST00000542794.5:c.*453C=	ENSP00000439983.1:n.*453C=
ENST00000543044.2:c.415C=	ENSP00000440219.1:p.Gln139=
ENST00000543265.1:c.*74C=	ENSP00000443660.1:n.*74C=
ENST00000544025.5:n.465+7908C=
ENST00000544801.5:c.370+7908C=	ENSP00000442581.1:n.370+7908C=
ENST00000544880.1:n.374+7908C=
NM_017841.2:c.451C= , LRG_519t1:c.451C=	NP_060311.1:p.Gln151=
NM_017841.4:c.451C= MANE Select	NP_060311.1:p.Gln151=