Canonical Allele Identifier: CA1977301336
Gene: SDHAF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446249_61446253delinsCTCAT , CM000673.2:g.61446249_61446253delinsCTCAT GRCh38
NC_000011.9:g.61213721_61213725delinsCTCAT , CM000673.1:g.61213721_61213725delinsCTCAT GRCh37
NC_000011.8:g.60970297_60970301delinsCTCAT NCBI36
NG_023393.1:g.21125_21129delinsCTCAT , LRG_519:g.21125_21129delinsCTCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.*178_*182delinsCTCAT MANE Select ENSP00000301761.3:n.*178_*182delinsCTCAT
ENST00000301761.6:c.*178_*182delinsCTCAT ENSP00000301761.2:n.*178_*182delinsCTCAT
ENST00000536670.5:n.396+8136_396+8140delinsCTCAT
ENST00000538594.5:c.370+8136_370+8140delinsCTCAT ENSP00000440939.1:n.370+8136_370+8140delinsCTCAT
ENST00000541135.5:c.377+8129_377+8133delinsCTCAT ENSP00000443130.1:n.377+8129_377+8133delinsCTCAT
ENST00000542074.1:c.*258_*262delinsCTCAT ENSP00000469670.1:n.*258_*262delinsCTCAT
ENST00000542794.5:c.*681_*685delinsCTCAT ENSP00000439983.1:n.*681_*685delinsCTCAT
ENST00000543044.2:c.*160+18_*160+22delinsCTCAT ENSP00000440219.1:n.*160+18_*160+22delinsCTCAT
ENST00000544025.5:n.465+8136_465+8140delinsCTCAT
ENST00000544801.5:c.370+8136_370+8140delinsCTCAT ENSP00000442581.1:n.370+8136_370+8140delinsCTCAT
ENST00000544880.1:n.374+8136_374+8140delinsCTCAT
NM_017841.2:c.*178_*182delinsCTCAT , LRG_519t1:c.*178_*182delinsCTCAT NP_060311.1:n.*178_*182delinsCTCAT
NM_017841.4:c.*178_*182delinsCTCAT MANE Select NP_060311.1:n.*178_*182delinsCTCAT