Canonical Allele Identifier: CA1977300631

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61445675C= , CM000673.2:g.61445675C=	GRCh38
NC_000011.9:g.61213147C= , CM000673.1:g.61213147C=	GRCh37
NC_000011.8:g.60969723C=	NCBI36
NG_023393.1:g.20551C= , LRG_519:g.20551C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.371-266C= MANE Select	ENSP00000301761.3:n.371-266C=
ENST00000301761.6:c.371-266C=	ENSP00000301761.2:n.371-266C=
ENST00000359614.9:c.*79-266C=	ENSP00000352630.5:n.*79-266C=
ENST00000536670.5:n.396+7562C=
ENST00000537782.5:c.*17-266C=	ENSP00000469951.1:n.*17-266C=
ENST00000538594.5:c.370+7562C=	ENSP00000440939.1:n.370+7562C=
ENST00000541135.5:c.377+7555C=	ENSP00000443130.1:n.377+7555C=
ENST00000542074.1:c.37-266C=	ENSP00000469670.1:n.37-266C=
ENST00000542794.5:c.*373-266C=	ENSP00000439983.1:n.*373-266C=
ENST00000543044.2:c.335-266C=	ENSP00000440219.1:n.335-266C=
ENST00000543265.1:c.261-266C=	ENSP00000443660.1:n.261-266C=
ENST00000544025.5:n.465+7562C=
ENST00000544801.5:c.370+7562C=	ENSP00000442581.1:n.370+7562C=
ENST00000544880.1:n.374+7562C=
NM_017841.2:c.371-266C= , LRG_519t1:c.371-266C=	NP_060311.1:n.371-266C=
NM_017841.4:c.371-266C= MANE Select	NP_060311.1:n.371-266C=