Canonical Allele Identifier: CA1977301175
Gene: SDHAF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446091C= , CM000673.2:g.61446091C= GRCh38
NC_000011.9:g.61213563C= , CM000673.1:g.61213563C= GRCh37
NC_000011.8:g.60970139C= NCBI36
NG_023393.1:g.20967C= , LRG_519:g.20967C=

Transcript Alleles

HGVS Amino-acid change
ENST00000301761.7:c.*20C= MANE Select ENSP00000301761.3:n.*20C=
ENST00000301761.6:c.*20C= ENSP00000301761.2:n.*20C=
ENST00000536670.5:n.396+7978C=
ENST00000538594.5:c.370+7978C= ENSP00000440939.1:n.370+7978C=
ENST00000541135.5:c.377+7971C= ENSP00000443130.1:n.377+7971C=
ENST00000542074.1:c.*100C= ENSP00000469670.1:n.*100C=
ENST00000542794.5:c.*523C= ENSP00000439983.1:n.*523C=
ENST00000543044.2:c.*20C= ENSP00000440219.1:n.*20C=
ENST00000543265.1:c.*144C= ENSP00000443660.1:n.*144C=
ENST00000544025.5:n.465+7978C=
ENST00000544801.5:c.370+7978C= ENSP00000442581.1:n.370+7978C=
ENST00000544880.1:n.374+7978C=
NM_017841.2:c.*20C= , LRG_519t1:c.*20C= NP_060311.1:n.*20C=
NM_017841.4:c.*20C= MANE Select NP_060311.1:n.*20C=