Canonical Allele Identifier: CA1977301063

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446043T= , CM000673.2:g.61446043T=	GRCh38
NC_000011.9:g.61213515T= , CM000673.1:g.61213515T=	GRCh37
NC_000011.8:g.60970091T=	NCBI36
NG_023393.1:g.20919T= , LRG_519:g.20919T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.473T= MANE Select	ENSP00000301761.3:p.Leu158=
ENST00000301761.6:c.473T=	ENSP00000301761.2:p.Leu158=
ENST00000536670.5:n.396+7930T=
ENST00000537782.5:c.*119T=	ENSP00000469951.1:n.*119T=
ENST00000538594.5:c.370+7930T=	ENSP00000440939.1:n.370+7930T=
ENST00000541135.5:c.377+7923T=	ENSP00000443130.1:n.377+7923T=
ENST00000542074.1:c.*52T=	ENSP00000469670.1:n.*52T=
ENST00000542794.5:c.*475T=	ENSP00000439983.1:n.*475T=
ENST00000543044.2:c.437T=	ENSP00000440219.1:p.Leu146=
ENST00000543265.1:c.*96T=	ENSP00000443660.1:n.*96T=
ENST00000544025.5:n.465+7930T=
ENST00000544801.5:c.370+7930T=	ENSP00000442581.1:n.370+7930T=
ENST00000544880.1:n.374+7930T=
NM_017841.2:c.473T= , LRG_519t1:c.473T=	NP_060311.1:p.Leu158=
NM_017841.4:c.473T= MANE Select	NP_060311.1:p.Leu158=