Canonical Allele Identifier: CA6035174

Gene: SDHAF2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61438010del , CM000673.2:g.61438010del	GRCh38
NC_000011.9:g.61205482del , CM000673.1:g.61205482del	GRCh37
NC_000011.8:g.60962058del	NCBI36
NG_023393.1:g.12886del , LRG_519:g.12886del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.267del MANE Select	ENSP00000301761.3:p.Phe89LeufsTer9
ENST00000301761.6:c.267del	ENSP00000301761.2:p.Phe89LeufsTer9
ENST00000359614.9:c.267del	ENSP00000352630.5:p.Phe89LeufsTer9
ENST00000534878.5:c.267del	ENSP00000471030.1:p.Phe89LeufsTer9
ENST00000536250.1:c.*269del	ENSP00000471120.1:n.*269del
ENST00000536670.5:n.293del
ENST00000537782.5:c.267del	ENSP00000469951.1:p.Phe89LeufsTer9
ENST00000538594.5:c.267del	ENSP00000440939.1:p.Phe89LeufsTer9
ENST00000541135.5:c.267del	ENSP00000443130.1:p.Phe89LeufsTer9
ENST00000542074.1:c.36+7828del	ENSP00000469670.1:n.36+7828del
ENST00000542794.5:c.*269del	ENSP00000439983.1:n.*269del
ENST00000543044.2:c.231del	ENSP00000440219.1:p.Phe77LeufsTer9
ENST00000543265.1:c.260+162del	ENSP00000443660.1:n.260+162del
ENST00000544025.5:n.362del
ENST00000544801.5:c.267del	ENSP00000442581.1:p.Phe89LeufsTer9
ENST00000544880.1:n.271del
NM_017841.2:c.267del , LRG_519t1:c.267del	NP_060311.1:p.Phe89LeufsTer9
NM_017841.4:c.267del MANE Select	NP_060311.1:p.Phe89LeufsTer9