Canonical Allele Identifier: CA2613853004
Gene: SDHAF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61437864_61437865insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG , CM000673.2:g.61437864_61437865insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG GRCh38
NC_000011.9:g.61205336_61205337insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG , CM000673.1:g.61205336_61205337insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG GRCh37
NC_000011.8:g.60961912_60961913insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG NCBI36
NG_023393.1:g.12740_12741insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG , LRG_519:g.12740_12741insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG MANE Select ENSP00000301761.3:n.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGC...
ENST00000301761.6:c.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG ENSP00000301761.2:n.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGC...
ENST00000359614.9:c.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG ENSP00000352630.5:n.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGC...
ENST00000534878.5:c.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG ENSP00000471030.1:n.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGC...
ENST00000536250.1:c.*262+16_*262+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG ENSP00000471120.1:n.*262+16_*262+17insGGTGGGGCATGCCTGTAATCCCA...
ENST00000536670.5:n.286+16_286+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG
ENST00000537782.5:c.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG ENSP00000469951.1:n.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGC...
ENST00000538594.5:c.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG ENSP00000440939.1:n.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGC...
ENST00000541135.5:c.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG ENSP00000443130.1:n.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGC...
ENST00000542074.1:c.36+7682_36+7683insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG ENSP00000469670.1:n.36+7682_36+7683insGGTGGGGCATGCCTGTAATCCCA...
ENST00000542794.5:c.*262+16_*262+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG ENSP00000439983.1:n.*262+16_*262+17insGGTGGGGCATGCCTGTAATCCCA...
ENST00000543044.2:c.224+16_224+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG ENSP00000440219.1:n.224+16_224+17insGGTGGGGCATGCCTGTAATCCCAGC...
ENST00000543265.1:c.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG ENSP00000443660.1:n.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGC...
ENST00000544025.5:n.355+16_355+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG
ENST00000544801.5:c.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG ENSP00000442581.1:n.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGC...
ENST00000544880.1:n.264+16_264+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG
NM_017841.2:c.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG , LRG_519t1:c.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG NP_060311.1:n.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCG...
NM_017841.4:c.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGG MANE Select NP_060311.1:n.260+16_260+17insGGTGGGGCATGCCTGTAATCCCAGCTACTCG...