Canonical Allele Identifier: CA1977293810

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61437818G= , CM000673.2:g.61437818G=	GRCh38
NC_000011.9:g.61205290G= , CM000673.1:g.61205290G=	GRCh37
NC_000011.8:g.60961866G=	NCBI36
NG_023393.1:g.12694G= , LRG_519:g.12694G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.230G= MANE Select	ENSP00000301761.3:p.Arg77=
ENST00000301761.6:c.230G=	ENSP00000301761.2:p.Arg77=
ENST00000359614.9:c.230G=	ENSP00000352630.5:p.Arg77=
ENST00000534878.5:c.230G=	ENSP00000471030.1:p.Arg77=
ENST00000536250.1:c.*232G=	ENSP00000471120.1:n.*232G=
ENST00000536670.5:n.256G=
ENST00000537782.5:c.230G=	ENSP00000469951.1:p.Arg77=
ENST00000538594.5:c.230G=	ENSP00000440939.1:p.Arg77=
ENST00000541135.5:c.230G=	ENSP00000443130.1:p.Arg77=
ENST00000542074.1:c.36+7636G=	ENSP00000469670.1:n.36+7636G=
ENST00000542794.5:c.*232G=	ENSP00000439983.1:n.*232G=
ENST00000543044.2:c.194G=	ENSP00000440219.1:p.Arg65=
ENST00000543265.1:c.230G=	ENSP00000443660.1:p.Arg77=
ENST00000544025.5:n.325G=
ENST00000544801.5:c.230G=	ENSP00000442581.1:p.Arg77=
ENST00000544880.1:n.234G=
NM_017841.2:c.230G= , LRG_519t1:c.230G=	NP_060311.1:p.Arg77=
NM_017841.4:c.230G= MANE Select	NP_060311.1:p.Arg77=