Canonical Allele Identifier: CA1977301047

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446035C= , CM000673.2:g.61446035C=	GRCh38
NC_000011.9:g.61213507C= , CM000673.1:g.61213507C=	GRCh37
NC_000011.8:g.60970083C=	NCBI36
NG_023393.1:g.20911C= , LRG_519:g.20911C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.465C= MANE Select	ENSP00000301761.3:p.Ala155=
ENST00000301761.6:c.465C=	ENSP00000301761.2:p.Ala155=
ENST00000536670.5:n.396+7922C=
ENST00000537782.5:c.*111C=	ENSP00000469951.1:n.*111C=
ENST00000538594.5:c.370+7922C=	ENSP00000440939.1:n.370+7922C=
ENST00000541135.5:c.377+7915C=	ENSP00000443130.1:n.377+7915C=
ENST00000542074.1:c.*44C=	ENSP00000469670.1:n.*44C=
ENST00000542794.5:c.*467C=	ENSP00000439983.1:n.*467C=
ENST00000543044.2:c.429C=	ENSP00000440219.1:p.Ala143=
ENST00000543265.1:c.*88C=	ENSP00000443660.1:n.*88C=
ENST00000544025.5:n.465+7922C=
ENST00000544801.5:c.370+7922C=	ENSP00000442581.1:n.370+7922C=
ENST00000544880.1:n.374+7922C=
NM_017841.2:c.465C= , LRG_519t1:c.465C=	NP_060311.1:p.Ala155=
NM_017841.4:c.465C= MANE Select	NP_060311.1:p.Ala155=