Canonical Allele Identifier: CA1977293834
Gene: SDHAF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61437864T= , CM000673.2:g.61437864T= GRCh38
NC_000011.9:g.61205336T= , CM000673.1:g.61205336T= GRCh37
NC_000011.8:g.60961912T= NCBI36
NG_023393.1:g.12740T= , LRG_519:g.12740T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.260+16T= MANE Select ENSP00000301761.3:n.260+16T=
ENST00000301761.6:c.260+16T= ENSP00000301761.2:n.260+16T=
ENST00000359614.9:c.260+16T= ENSP00000352630.5:n.260+16T=
ENST00000534878.5:c.260+16T= ENSP00000471030.1:n.260+16T=
ENST00000536250.1:c.*262+16T= ENSP00000471120.1:n.*262+16T=
ENST00000536670.5:n.286+16T=
ENST00000537782.5:c.260+16T= ENSP00000469951.1:n.260+16T=
ENST00000538594.5:c.260+16T= ENSP00000440939.1:n.260+16T=
ENST00000541135.5:c.260+16T= ENSP00000443130.1:n.260+16T=
ENST00000542074.1:c.36+7682T= ENSP00000469670.1:n.36+7682T=
ENST00000542794.5:c.*262+16T= ENSP00000439983.1:n.*262+16T=
ENST00000543044.2:c.224+16T= ENSP00000440219.1:n.224+16T=
ENST00000543265.1:c.260+16T= ENSP00000443660.1:n.260+16T=
ENST00000544025.5:n.355+16T=
ENST00000544801.5:c.260+16T= ENSP00000442581.1:n.260+16T=
ENST00000544880.1:n.264+16T=
NM_017841.2:c.260+16T= , LRG_519t1:c.260+16T= NP_060311.1:n.260+16T=
NM_017841.4:c.260+16T= MANE Select NP_060311.1:n.260+16T=