Canonical Allele Identifier: CA1977293793

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61437787A= , CM000673.2:g.61437787A=	GRCh38
NC_000011.9:g.61205259A= , CM000673.1:g.61205259A=	GRCh37
NC_000011.8:g.60961835A=	NCBI36
NG_023393.1:g.12663A= , LRG_519:g.12663A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.199A= MANE Select	ENSP00000301761.3:p.Arg67=
ENST00000301761.6:c.199A=	ENSP00000301761.2:p.Arg67=
ENST00000359614.9:c.199A=	ENSP00000352630.5:p.Arg67=
ENST00000534878.5:c.199A=	ENSP00000471030.1:p.Arg67=
ENST00000536250.1:c.*201A=	ENSP00000471120.1:n.*201A=
ENST00000536670.5:n.225A=
ENST00000537782.5:c.199A=	ENSP00000469951.1:p.Arg67=
ENST00000538594.5:c.199A=	ENSP00000440939.1:p.Arg67=
ENST00000541135.5:c.199A=	ENSP00000443130.1:p.Arg67=
ENST00000542074.1:c.36+7605A=	ENSP00000469670.1:n.36+7605A=
ENST00000542794.5:c.*201A=	ENSP00000439983.1:n.*201A=
ENST00000543044.2:c.163A=	ENSP00000440219.1:p.Arg55=
ENST00000543265.1:c.199A=	ENSP00000443660.1:p.Arg67=
ENST00000544025.5:n.294A=
ENST00000544801.5:c.199A=	ENSP00000442581.1:p.Arg67=
ENST00000544880.1:n.203A=
NM_017841.2:c.199A= , LRG_519t1:c.199A=	NP_060311.1:p.Arg67=
NM_017841.4:c.199A= MANE Select	NP_060311.1:p.Arg67=