Canonical Allele Identifier: CA1977300805

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61445919T= , CM000673.2:g.61445919T=	GRCh38
NC_000011.9:g.61213391T= , CM000673.1:g.61213391T=	GRCh37
NC_000011.8:g.60969967T=	NCBI36
NG_023393.1:g.20795T= , LRG_519:g.20795T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.371-22T= MANE Select	ENSP00000301761.3:n.371-22T=
ENST00000301761.6:c.371-22T=	ENSP00000301761.2:n.371-22T=
ENST00000359614.9:c.*79-22T=	ENSP00000352630.5:n.*79-22T=
ENST00000536670.5:n.396+7806T=
ENST00000537782.5:c.*17-22T=	ENSP00000469951.1:n.*17-22T=
ENST00000538594.5:c.370+7806T=	ENSP00000440939.1:n.370+7806T=
ENST00000541135.5:c.377+7799T=	ENSP00000443130.1:n.377+7799T=
ENST00000542074.1:c.37-22T=	ENSP00000469670.1:n.37-22T=
ENST00000542794.5:c.*373-22T=	ENSP00000439983.1:n.*373-22T=
ENST00000543044.2:c.335-22T=	ENSP00000440219.1:n.335-22T=
ENST00000543265.1:c.261-22T=	ENSP00000443660.1:n.261-22T=
ENST00000544025.5:n.465+7806T=
ENST00000544801.5:c.370+7806T=	ENSP00000442581.1:n.370+7806T=
ENST00000544880.1:n.374+7806T=
NM_017841.2:c.371-22T= , LRG_519t1:c.371-22T=	NP_060311.1:n.371-22T=
NM_017841.4:c.371-22T= MANE Select	NP_060311.1:n.371-22T=