Canonical Allele Identifier: CA1977300988

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446019A= , CM000673.2:g.61446019A=	GRCh38
NC_000011.9:g.61213491A= , CM000673.1:g.61213491A=	GRCh37
NC_000011.8:g.60970067A=	NCBI36
NG_023393.1:g.20895A= , LRG_519:g.20895A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.449A= MANE Select	ENSP00000301761.3:p.Glu150=
ENST00000301761.6:c.449A=	ENSP00000301761.2:p.Glu150=
ENST00000536670.5:n.396+7906A=
ENST00000537782.5:c.*95A=	ENSP00000469951.1:n.*95A=
ENST00000538594.5:c.370+7906A=	ENSP00000440939.1:n.370+7906A=
ENST00000541135.5:c.377+7899A=	ENSP00000443130.1:n.377+7899A=
ENST00000542074.1:c.*28A=	ENSP00000469670.1:n.*28A=
ENST00000542794.5:c.*451A=	ENSP00000439983.1:n.*451A=
ENST00000543044.2:c.413A=	ENSP00000440219.1:p.Glu138=
ENST00000543265.1:c.*72A=	ENSP00000443660.1:n.*72A=
ENST00000544025.5:n.465+7906A=
ENST00000544801.5:c.370+7906A=	ENSP00000442581.1:n.370+7906A=
ENST00000544880.1:n.374+7906A=
NM_017841.2:c.449A= , LRG_519t1:c.449A=	NP_060311.1:p.Glu150=
NM_017841.4:c.449A= MANE Select	NP_060311.1:p.Glu150=