Canonical Allele Identifier: CA1977301158
Gene: SDHAF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446080C= , CM000673.2:g.61446080C= GRCh38
NC_000011.9:g.61213552C= , CM000673.1:g.61213552C= GRCh37
NC_000011.8:g.60970128C= NCBI36
NG_023393.1:g.20956C= , LRG_519:g.20956C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.*9C= MANE Select ENSP00000301761.3:n.*9C=
ENST00000301761.6:c.*9C= ENSP00000301761.2:n.*9C=
ENST00000536670.5:n.396+7967C=
ENST00000538594.5:c.370+7967C= ENSP00000440939.1:n.370+7967C=
ENST00000541135.5:c.377+7960C= ENSP00000443130.1:n.377+7960C=
ENST00000542074.1:c.*89C= ENSP00000469670.1:n.*89C=
ENST00000542794.5:c.*512C= ENSP00000439983.1:n.*512C=
ENST00000543044.2:c.*9C= ENSP00000440219.1:n.*9C=
ENST00000543265.1:c.*133C= ENSP00000443660.1:n.*133C=
ENST00000544025.5:n.465+7967C=
ENST00000544801.5:c.370+7967C= ENSP00000442581.1:n.370+7967C=
ENST00000544880.1:n.374+7967C=
NM_017841.2:c.*9C= , LRG_519t1:c.*9C= NP_060311.1:n.*9C=
NM_017841.4:c.*9C= MANE Select NP_060311.1:n.*9C=