Canonical Allele Identifier: CA1977301183
Gene: SDHAF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446097G= , CM000673.2:g.61446097G= GRCh38
NC_000011.9:g.61213569G= , CM000673.1:g.61213569G= GRCh37
NC_000011.8:g.60970145G= NCBI36
NG_023393.1:g.20973G= , LRG_519:g.20973G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.*26G= MANE Select ENSP00000301761.3:n.*26G=
ENST00000301761.6:c.*26G= ENSP00000301761.2:n.*26G=
ENST00000536670.5:n.396+7984G=
ENST00000538594.5:c.370+7984G= ENSP00000440939.1:n.370+7984G=
ENST00000541135.5:c.377+7977G= ENSP00000443130.1:n.377+7977G=
ENST00000542074.1:c.*106G= ENSP00000469670.1:n.*106G=
ENST00000542794.5:c.*529G= ENSP00000439983.1:n.*529G=
ENST00000543044.2:c.*26G= ENSP00000440219.1:n.*26G=
ENST00000543265.1:c.*150G= ENSP00000443660.1:n.*150G=
ENST00000544025.5:n.465+7984G=
ENST00000544801.5:c.370+7984G= ENSP00000442581.1:n.370+7984G=
ENST00000544880.1:n.374+7984G=
NM_017841.2:c.*26G= , LRG_519t1:c.*26G= NP_060311.1:n.*26G=
NM_017841.4:c.*26G= MANE Select NP_060311.1:n.*26G=