Canonical Allele Identifier: CA474523437

Gene: SDHAF2

Linked Data

• MyVariant Identifiers: chr11:g.61213465A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61445993A>G , CM000673.2:g.61445993A>G	GRCh38
NC_000011.9:g.61213465A>G , CM000673.1:g.61213465A>G	GRCh37
NC_000011.8:g.60970041A>G	NCBI36
NG_023393.1:g.20869A>G , LRG_519:g.20869A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.423A>G MANE Select	ENSP00000301761.3:p.Arg141=
ENST00000301761.6:c.423A>G	ENSP00000301761.2:p.Arg141=
ENST00000359614.9:c.*131A>G	ENSP00000352630.5:n.*131A>G
ENST00000536670.5:n.396+7880A>G
ENST00000537782.5:c.*69A>G	ENSP00000469951.1:n.*69A>G
ENST00000538594.5:c.370+7880A>G	ENSP00000440939.1:n.370+7880A>G
ENST00000541135.5:c.377+7873A>G	ENSP00000443130.1:n.377+7873A>G
ENST00000542074.1:c.*2A>G	ENSP00000469670.1:n.*2A>G
ENST00000542794.5:c.*425A>G	ENSP00000439983.1:n.*425A>G
ENST00000543044.2:c.387A>G	ENSP00000440219.1:p.Arg129=
ENST00000543265.1:c.*46A>G	ENSP00000443660.1:n.*46A>G
ENST00000544025.5:n.465+7880A>G
ENST00000544801.5:c.370+7880A>G	ENSP00000442581.1:n.370+7880A>G
ENST00000544880.1:n.374+7880A>G
NM_017841.2:c.423A>G , LRG_519t1:c.423A>G	NP_060311.1:p.Arg141=
NM_017841.4:c.423A>G MANE Select	NP_060311.1:p.Arg141=