Canonical Allele Identifier: CA1977300918

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61445985C= , CM000673.2:g.61445985C=	GRCh38
NC_000011.9:g.61213457C= , CM000673.1:g.61213457C=	GRCh37
NC_000011.8:g.60970033C=	NCBI36
NG_023393.1:g.20861C= , LRG_519:g.20861C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.415C= MANE Select	ENSP00000301761.3:p.Leu139=
ENST00000301761.6:c.415C=	ENSP00000301761.2:p.Leu139=
ENST00000359614.9:c.*123C=	ENSP00000352630.5:n.*123C=
ENST00000536670.5:n.396+7872C=
ENST00000537782.5:c.*61C=	ENSP00000469951.1:n.*61C=
ENST00000538594.5:c.370+7872C=	ENSP00000440939.1:n.370+7872C=
ENST00000541135.5:c.377+7865C=	ENSP00000443130.1:n.377+7865C=
ENST00000542074.1:c.81C=	ENSP00000469670.1:p.Pro27=
ENST00000542794.5:c.*417C=	ENSP00000439983.1:n.*417C=
ENST00000543044.2:c.379C=	ENSP00000440219.1:p.Leu127=
ENST00000543265.1:c.*38C=	ENSP00000443660.1:n.*38C=
ENST00000544025.5:n.465+7872C=
ENST00000544801.5:c.370+7872C=	ENSP00000442581.1:n.370+7872C=
ENST00000544880.1:n.374+7872C=
NM_017841.2:c.415C= , LRG_519t1:c.415C=	NP_060311.1:p.Leu139=
NM_017841.4:c.415C= MANE Select	NP_060311.1:p.Leu139=