Canonical Allele Identifier: CA1977301121
Gene: SDHAF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446066C= , CM000673.2:g.61446066C= GRCh38
NC_000011.9:g.61213538C= , CM000673.1:g.61213538C= GRCh37
NC_000011.8:g.60970114C= NCBI36
NG_023393.1:g.20942C= , LRG_519:g.20942C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.496C= MANE Select ENSP00000301761.3:p.Arg166=
ENST00000301761.6:c.496C= ENSP00000301761.2:p.Arg166=
ENST00000536670.5:n.396+7953C=
ENST00000538594.5:c.370+7953C= ENSP00000440939.1:n.370+7953C=
ENST00000541135.5:c.377+7946C= ENSP00000443130.1:n.377+7946C=
ENST00000542074.1:c.*75C= ENSP00000469670.1:n.*75C=
ENST00000542794.5:c.*498C= ENSP00000439983.1:n.*498C=
ENST00000543044.2:c.460C= ENSP00000440219.1:p.Arg154=
ENST00000543265.1:c.*119C= ENSP00000443660.1:n.*119C=
ENST00000544025.5:n.465+7953C=
ENST00000544801.5:c.370+7953C= ENSP00000442581.1:n.370+7953C=
ENST00000544880.1:n.374+7953C=
NM_017841.2:c.496C= , LRG_519t1:c.496C= NP_060311.1:p.Arg166=
NM_017841.4:c.496C= MANE Select NP_060311.1:p.Arg166=