Canonical Allele Identifier: CA1977293838

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61437870T= , CM000673.2:g.61437870T=	GRCh38
NC_000011.9:g.61205342T= , CM000673.1:g.61205342T=	GRCh37
NC_000011.8:g.60961918T=	NCBI36
NG_023393.1:g.12746T= , LRG_519:g.12746T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.260+22T= MANE Select	ENSP00000301761.3:n.260+22T=
ENST00000301761.6:c.260+22T=	ENSP00000301761.2:n.260+22T=
ENST00000359614.9:c.260+22T=	ENSP00000352630.5:n.260+22T=
ENST00000534878.5:c.260+22T=	ENSP00000471030.1:n.260+22T=
ENST00000536250.1:c.*262+22T=	ENSP00000471120.1:n.*262+22T=
ENST00000536670.5:n.286+22T=
ENST00000537782.5:c.260+22T=	ENSP00000469951.1:n.260+22T=
ENST00000538594.5:c.260+22T=	ENSP00000440939.1:n.260+22T=
ENST00000541135.5:c.260+22T=	ENSP00000443130.1:n.260+22T=
ENST00000542074.1:c.36+7688T=	ENSP00000469670.1:n.36+7688T=
ENST00000542794.5:c.*262+22T=	ENSP00000439983.1:n.*262+22T=
ENST00000543044.2:c.224+22T=	ENSP00000440219.1:n.224+22T=
ENST00000543265.1:c.260+22T=	ENSP00000443660.1:n.260+22T=
ENST00000544025.5:n.355+22T=
ENST00000544801.5:c.260+22T=	ENSP00000442581.1:n.260+22T=
ENST00000544880.1:n.264+22T=
NM_017841.2:c.260+22T= , LRG_519t1:c.260+22T=	NP_060311.1:n.260+22T=
NM_017841.4:c.260+22T= MANE Select	NP_060311.1:n.260+22T=