Canonical Allele Identifier: CA1977300934

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61445991A= , CM000673.2:g.61445991A=	GRCh38
NC_000011.9:g.61213463A= , CM000673.1:g.61213463A=	GRCh37
NC_000011.8:g.60970039A=	NCBI36
NG_023393.1:g.20867A= , LRG_519:g.20867A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.421A= MANE Select	ENSP00000301761.3:p.Arg141=
ENST00000301761.6:c.421A=	ENSP00000301761.2:p.Arg141=
ENST00000359614.9:c.*129A=	ENSP00000352630.5:n.*129A=
ENST00000536670.5:n.396+7878A=
ENST00000537782.5:c.*67A=	ENSP00000469951.1:n.*67A=
ENST00000538594.5:c.370+7878A=	ENSP00000440939.1:n.370+7878A=
ENST00000541135.5:c.377+7871A=	ENSP00000443130.1:n.377+7871A=
ENST00000542074.1:c.87A=	ENSP00000469670.1:p.Ter29=
ENST00000542794.5:c.*423A=	ENSP00000439983.1:n.*423A=
ENST00000543044.2:c.385A=	ENSP00000440219.1:p.Arg129=
ENST00000543265.1:c.*44A=	ENSP00000443660.1:n.*44A=
ENST00000544025.5:n.465+7878A=
ENST00000544801.5:c.370+7878A=	ENSP00000442581.1:n.370+7878A=
ENST00000544880.1:n.374+7878A=
NM_017841.2:c.421A= , LRG_519t1:c.421A=	NP_060311.1:p.Arg141=
NM_017841.4:c.421A= MANE Select	NP_060311.1:p.Arg141=