Canonical Allele Identifier: CA2613847798
Gene: SDHAF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446413_61446414insGT , CM000673.2:g.61446413_61446414insGT GRCh38
NC_000011.9:g.61213885_61213886insGT , CM000673.1:g.61213885_61213886insGT GRCh37
NC_000011.8:g.60970461_60970462insGT NCBI36
NG_023393.1:g.21289_21290insGT , LRG_519:g.21289_21290insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.*342_*343insGT MANE Select ENSP00000301761.3:n.*342_*343insGT
ENST00000301761.6:c.*342_*343insGT ENSP00000301761.2:n.*342_*343insGT
ENST00000536670.5:n.396+8300_396+8301insGT
ENST00000538594.5:c.370+8300_370+8301insGT ENSP00000440939.1:n.370+8300_370+8301insGT
ENST00000541135.5:c.377+8293_377+8294insGT ENSP00000443130.1:n.377+8293_377+8294insGT
ENST00000542074.1:c.*422_*423insGT ENSP00000469670.1:n.*422_*423insGT
ENST00000543044.2:c.*160+182_*160+183insGT ENSP00000440219.1:n.*160+182_*160+183insGT
ENST00000544025.5:n.465+8300_465+8301insGT
ENST00000544801.5:c.370+8300_370+8301insGT ENSP00000442581.1:n.370+8300_370+8301insGT
ENST00000544880.1:n.374+8300_374+8301insGT
NM_017841.2:c.*342_*343insGT , LRG_519t1:c.*342_*343insGT NP_060311.1:n.*342_*343insGT
NM_017841.4:c.*342_*343insGT MANE Select NP_060311.1:n.*342_*343insGT