Canonical Allele Identifier: CA1977301166
Gene: SDHAF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446084G= , CM000673.2:g.61446084G= GRCh38
NC_000011.9:g.61213556G= , CM000673.1:g.61213556G= GRCh37
NC_000011.8:g.60970132G= NCBI36
NG_023393.1:g.20960G= , LRG_519:g.20960G=

Transcript Alleles

HGVS Amino-acid change
ENST00000301761.7:c.*13G= MANE Select ENSP00000301761.3:n.*13G=
ENST00000301761.6:c.*13G= ENSP00000301761.2:n.*13G=
ENST00000536670.5:n.396+7971G=
ENST00000538594.5:c.370+7971G= ENSP00000440939.1:n.370+7971G=
ENST00000541135.5:c.377+7964G= ENSP00000443130.1:n.377+7964G=
ENST00000542074.1:c.*93G= ENSP00000469670.1:n.*93G=
ENST00000542794.5:c.*516G= ENSP00000439983.1:n.*516G=
ENST00000543044.2:c.*13G= ENSP00000440219.1:n.*13G=
ENST00000543265.1:c.*137G= ENSP00000443660.1:n.*137G=
ENST00000544025.5:n.465+7971G=
ENST00000544801.5:c.370+7971G= ENSP00000442581.1:n.370+7971G=
ENST00000544880.1:n.374+7971G=
NM_017841.2:c.*13G= , LRG_519t1:c.*13G= NP_060311.1:n.*13G=
NM_017841.4:c.*13G= MANE Select NP_060311.1:n.*13G=