Canonical Allele Identifier: CA1977300622

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61445664G= , CM000673.2:g.61445664G=	GRCh38
NC_000011.9:g.61213136G= , CM000673.1:g.61213136G=	GRCh37
NC_000011.8:g.60969712G=	NCBI36
NG_023393.1:g.20540G= , LRG_519:g.20540G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.371-277G= MANE Select	ENSP00000301761.3:n.371-277G=
ENST00000301761.6:c.371-277G=	ENSP00000301761.2:n.371-277G=
ENST00000359614.9:c.*79-277G=	ENSP00000352630.5:n.*79-277G=
ENST00000536670.5:n.396+7551G=
ENST00000537782.5:c.*17-277G=	ENSP00000469951.1:n.*17-277G=
ENST00000538594.5:c.370+7551G=	ENSP00000440939.1:n.370+7551G=
ENST00000541135.5:c.377+7544G=	ENSP00000443130.1:n.377+7544G=
ENST00000542074.1:c.37-277G=	ENSP00000469670.1:n.37-277G=
ENST00000542794.5:c.*373-277G=	ENSP00000439983.1:n.*373-277G=
ENST00000543044.2:c.335-277G=	ENSP00000440219.1:n.335-277G=
ENST00000543265.1:c.261-277G=	ENSP00000443660.1:n.261-277G=
ENST00000544025.5:n.465+7551G=
ENST00000544801.5:c.370+7551G=	ENSP00000442581.1:n.370+7551G=
ENST00000544880.1:n.374+7551G=
NM_017841.2:c.371-277G= , LRG_519t1:c.371-277G=	NP_060311.1:n.371-277G=
NM_017841.4:c.371-277G= MANE Select	NP_060311.1:n.371-277G=