Canonical Allele Identifier: CA1977300978

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446016A= , CM000673.2:g.61446016A=	GRCh38
NC_000011.9:g.61213488A= , CM000673.1:g.61213488A=	GRCh37
NC_000011.8:g.60970064A=	NCBI36
NG_023393.1:g.20892A= , LRG_519:g.20892A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.446A= MANE Select	ENSP00000301761.3:p.Lys149=
ENST00000301761.6:c.446A=	ENSP00000301761.2:p.Lys149=
ENST00000536670.5:n.396+7903A=
ENST00000537782.5:c.*92A=	ENSP00000469951.1:n.*92A=
ENST00000538594.5:c.370+7903A=	ENSP00000440939.1:n.370+7903A=
ENST00000541135.5:c.377+7896A=	ENSP00000443130.1:n.377+7896A=
ENST00000542074.1:c.*25A=	ENSP00000469670.1:n.*25A=
ENST00000542794.5:c.*448A=	ENSP00000439983.1:n.*448A=
ENST00000543044.2:c.410A=	ENSP00000440219.1:p.Lys137=
ENST00000543265.1:c.*69A=	ENSP00000443660.1:n.*69A=
ENST00000544025.5:n.465+7903A=
ENST00000544801.5:c.370+7903A=	ENSP00000442581.1:n.370+7903A=
ENST00000544880.1:n.374+7903A=
NM_017841.2:c.446A= , LRG_519t1:c.446A=	NP_060311.1:p.Lys149=
NM_017841.4:c.446A= MANE Select	NP_060311.1:p.Lys149=