Canonical Allele Identifier: CA1977300931

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61445990G= , CM000673.2:g.61445990G=	GRCh38
NC_000011.9:g.61213462G= , CM000673.1:g.61213462G=	GRCh37
NC_000011.8:g.60970038G=	NCBI36
NG_023393.1:g.20866G= , LRG_519:g.20866G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.420G= MANE Select	ENSP00000301761.3:p.Leu140=
ENST00000301761.6:c.420G=	ENSP00000301761.2:p.Leu140=
ENST00000359614.9:c.*128G=	ENSP00000352630.5:n.*128G=
ENST00000536670.5:n.396+7877G=
ENST00000537782.5:c.*66G=	ENSP00000469951.1:n.*66G=
ENST00000538594.5:c.370+7877G=	ENSP00000440939.1:n.370+7877G=
ENST00000541135.5:c.377+7870G=	ENSP00000443130.1:n.377+7870G=
ENST00000542074.1:c.86G=	ENSP00000469670.1:p.Ter29=
ENST00000542794.5:c.*422G=	ENSP00000439983.1:n.*422G=
ENST00000543044.2:c.384G=	ENSP00000440219.1:p.Leu128=
ENST00000543265.1:c.*43G=	ENSP00000443660.1:n.*43G=
ENST00000544025.5:n.465+7877G=
ENST00000544801.5:c.370+7877G=	ENSP00000442581.1:n.370+7877G=
ENST00000544880.1:n.374+7877G=
NM_017841.2:c.420G= , LRG_519t1:c.420G=	NP_060311.1:p.Leu140=
NM_017841.4:c.420G= MANE Select	NP_060311.1:p.Leu140=