Canonical Allele Identifier: CA1977301162
Gene: SDHAF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446083C= , CM000673.2:g.61446083C= GRCh38
NC_000011.9:g.61213555C= , CM000673.1:g.61213555C= GRCh37
NC_000011.8:g.60970131C= NCBI36
NG_023393.1:g.20959C= , LRG_519:g.20959C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.*12C= MANE Select ENSP00000301761.3:n.*12C=
ENST00000301761.6:c.*12C= ENSP00000301761.2:n.*12C=
ENST00000536670.5:n.396+7970C=
ENST00000538594.5:c.370+7970C= ENSP00000440939.1:n.370+7970C=
ENST00000541135.5:c.377+7963C= ENSP00000443130.1:n.377+7963C=
ENST00000542074.1:c.*92C= ENSP00000469670.1:n.*92C=
ENST00000542794.5:c.*515C= ENSP00000439983.1:n.*515C=
ENST00000543044.2:c.*12C= ENSP00000440219.1:n.*12C=
ENST00000543265.1:c.*136C= ENSP00000443660.1:n.*136C=
ENST00000544025.5:n.465+7970C=
ENST00000544801.5:c.370+7970C= ENSP00000442581.1:n.370+7970C=
ENST00000544880.1:n.374+7970C=
NM_017841.2:c.*12C= , LRG_519t1:c.*12C= NP_060311.1:n.*12C=
NM_017841.4:c.*12C= MANE Select NP_060311.1:n.*12C=