Canonical Allele Identifier: CA1977300844

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61445949C= , CM000673.2:g.61445949C=	GRCh38
NC_000011.9:g.61213421C= , CM000673.1:g.61213421C=	GRCh37
NC_000011.8:g.60969997C=	NCBI36
NG_023393.1:g.20825C= , LRG_519:g.20825C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.379C= MANE Select	ENSP00000301761.3:p.Pro127=
ENST00000301761.6:c.379C=	ENSP00000301761.2:p.Pro127=
ENST00000359614.9:c.*87C=	ENSP00000352630.5:n.*87C=
ENST00000536670.5:n.396+7836C=
ENST00000537782.5:c.*25C=	ENSP00000469951.1:n.*25C=
ENST00000538594.5:c.370+7836C=	ENSP00000440939.1:n.370+7836C=
ENST00000541135.5:c.377+7829C=	ENSP00000443130.1:n.377+7829C=
ENST00000542074.1:c.45C=	ENSP00000469670.1:p.Asn15=
ENST00000542794.5:c.*381C=	ENSP00000439983.1:n.*381C=
ENST00000543044.2:c.343C=	ENSP00000440219.1:p.Pro115=
ENST00000543265.1:c.*2C=	ENSP00000443660.1:n.*2C=
ENST00000544025.5:n.465+7836C=
ENST00000544801.5:c.370+7836C=	ENSP00000442581.1:n.370+7836C=
ENST00000544880.1:n.374+7836C=
NM_017841.2:c.379C= , LRG_519t1:c.379C=	NP_060311.1:p.Pro127=
NM_017841.4:c.379C= MANE Select	NP_060311.1:p.Pro127=