Canonical Allele Identifier: CA1977301086

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446050C= , CM000673.2:g.61446050C=	GRCh38
NC_000011.9:g.61213522C= , CM000673.1:g.61213522C=	GRCh37
NC_000011.8:g.60970098C=	NCBI36
NG_023393.1:g.20926C= , LRG_519:g.20926C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.480C= MANE Select	ENSP00000301761.3:p.Tyr160=
ENST00000301761.6:c.480C=	ENSP00000301761.2:p.Tyr160=
ENST00000536670.5:n.396+7937C=
ENST00000537782.5:c.*126C=	ENSP00000469951.1:n.*126C=
ENST00000538594.5:c.370+7937C=	ENSP00000440939.1:n.370+7937C=
ENST00000541135.5:c.377+7930C=	ENSP00000443130.1:n.377+7930C=
ENST00000542074.1:c.*59C=	ENSP00000469670.1:n.*59C=
ENST00000542794.5:c.*482C=	ENSP00000439983.1:n.*482C=
ENST00000543044.2:c.444C=	ENSP00000440219.1:p.Tyr148=
ENST00000543265.1:c.*103C=	ENSP00000443660.1:n.*103C=
ENST00000544025.5:n.465+7937C=
ENST00000544801.5:c.370+7937C=	ENSP00000442581.1:n.370+7937C=
ENST00000544880.1:n.374+7937C=
NM_017841.2:c.480C= , LRG_519t1:c.480C=	NP_060311.1:p.Tyr160=
NM_017841.4:c.480C= MANE Select	NP_060311.1:p.Tyr160=