Canonical Allele Identifier: CA1977300848

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61445952G= , CM000673.2:g.61445952G=	GRCh38
NC_000011.9:g.61213424G= , CM000673.1:g.61213424G=	GRCh37
NC_000011.8:g.60970000G=	NCBI36
NG_023393.1:g.20828G= , LRG_519:g.20828G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.382G= MANE Select	ENSP00000301761.3:p.Ala128=
ENST00000301761.6:c.382G=	ENSP00000301761.2:p.Ala128=
ENST00000359614.9:c.*90G=	ENSP00000352630.5:n.*90G=
ENST00000536670.5:n.396+7839G=
ENST00000537782.5:c.*28G=	ENSP00000469951.1:n.*28G=
ENST00000538594.5:c.370+7839G=	ENSP00000440939.1:n.370+7839G=
ENST00000541135.5:c.377+7832G=	ENSP00000443130.1:n.377+7832G=
ENST00000542074.1:c.48G=	ENSP00000469670.1:p.Gln16=
ENST00000542794.5:c.*384G=	ENSP00000439983.1:n.*384G=
ENST00000543044.2:c.346G=	ENSP00000440219.1:p.Ala116=
ENST00000543265.1:c.*5G=	ENSP00000443660.1:n.*5G=
ENST00000544025.5:n.465+7839G=
ENST00000544801.5:c.370+7839G=	ENSP00000442581.1:n.370+7839G=
ENST00000544880.1:n.374+7839G=
NM_017841.2:c.382G= , LRG_519t1:c.382G=	NP_060311.1:p.Ala128=
NM_017841.4:c.382G= MANE Select	NP_060311.1:p.Ala128=