Canonical Allele Identifier: CA1977293933

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61438057A= , CM000673.2:g.61438057A=	GRCh38
NC_000011.9:g.61205529A= , CM000673.1:g.61205529A=	GRCh37
NC_000011.8:g.60962105A=	NCBI36
NG_023393.1:g.12933A= , LRG_519:g.12933A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.314A= MANE Select	ENSP00000301761.3:p.Tyr105=
ENST00000301761.6:c.314A=	ENSP00000301761.2:p.Tyr105=
ENST00000359614.9:c.314A=	ENSP00000352630.5:p.Tyr105=
ENST00000534878.5:c.314A=	ENSP00000471030.1:p.Tyr105=
ENST00000536250.1:c.*316A=	ENSP00000471120.1:n.*316A=
ENST00000536670.5:n.340A=
ENST00000537782.5:c.314A=	ENSP00000469951.1:p.Tyr105=
ENST00000538594.5:c.314A=	ENSP00000440939.1:p.Tyr105=
ENST00000541135.5:c.314A=	ENSP00000443130.1:p.Tyr105=
ENST00000542074.1:c.36+7875A=	ENSP00000469670.1:n.36+7875A=
ENST00000542794.5:c.*316A=	ENSP00000439983.1:n.*316A=
ENST00000543044.2:c.278A=	ENSP00000440219.1:p.Tyr93=
ENST00000543265.1:c.260+209A=	ENSP00000443660.1:n.260+209A=
ENST00000544025.5:n.409A=
ENST00000544801.5:c.314A=	ENSP00000442581.1:p.Tyr105=
ENST00000544880.1:n.318A=
NM_017841.2:c.314A= , LRG_519t1:c.314A=	NP_060311.1:p.Tyr105=
NM_017841.4:c.314A= MANE Select	NP_060311.1:p.Tyr105=