Canonical Allele Identifier: CA2574841567

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446002-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446007del , CM000673.2:g.61446007del	GRCh38
NC_000011.9:g.61213479del , CM000673.1:g.61213479del	GRCh37
NC_000011.8:g.60970055del	NCBI36
NG_023393.1:g.20883del , LRG_519:g.20883del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.437del MANE Select	ENSP00000301761.3:p.Asn146ThrfsTer?
ENST00000301761.6:c.437del	ENSP00000301761.2:p.Asn146ThrfsTer?
ENST00000536670.5:n.396+7894del
ENST00000537782.5:c.*83del	ENSP00000469951.1:n.*83del
ENST00000538594.5:c.370+7894del	ENSP00000440939.1:n.370+7894del
ENST00000541135.5:c.377+7887del	ENSP00000443130.1:n.377+7887del
ENST00000542074.1:c.*16del	ENSP00000469670.1:n.*16del
ENST00000542794.5:c.*439del	ENSP00000439983.1:n.*439del
ENST00000543044.2:c.401del	ENSP00000440219.1:p.Asn134ThrfsTer?
ENST00000543265.1:c.*60del	ENSP00000443660.1:n.*60del
ENST00000544025.5:n.465+7894del
ENST00000544801.5:c.370+7894del	ENSP00000442581.1:n.370+7894del
ENST00000544880.1:n.374+7894del
NM_017841.2:c.437del , LRG_519t1:c.437del	NP_060311.1:p.Asn146ThrfsTer?
NM_017841.4:c.437del MANE Select	NP_060311.1:p.Asn146ThrfsTer?