Canonical Allele Identifier: CA2613847256

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446038-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446039del , CM000673.2:g.61446039del	GRCh38
NC_000011.9:g.61213511del , CM000673.1:g.61213511del	GRCh37
NC_000011.8:g.60970087del	NCBI36
NG_023393.1:g.20915del , LRG_519:g.20915del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.469del MANE Select	ENSP00000301761.3:p.Asp157IlefsTer26
ENST00000301761.6:c.469del	ENSP00000301761.2:p.Asp157IlefsTer26
ENST00000536670.5:n.396+7926del
ENST00000537782.5:c.*115del	ENSP00000469951.1:n.*115del
ENST00000538594.5:c.370+7926del	ENSP00000440939.1:n.370+7926del
ENST00000541135.5:c.377+7919del	ENSP00000443130.1:n.377+7919del
ENST00000542074.1:c.*48del	ENSP00000469670.1:n.*48del
ENST00000542794.5:c.*471del	ENSP00000439983.1:n.*471del
ENST00000543044.2:c.433del	ENSP00000440219.1:p.Asp145IlefsTer26
ENST00000543265.1:c.*92del	ENSP00000443660.1:n.*92del
ENST00000544025.5:n.465+7926del
ENST00000544801.5:c.370+7926del	ENSP00000442581.1:n.370+7926del
ENST00000544880.1:n.374+7926del
NM_017841.2:c.469del , LRG_519t1:c.469del	NP_060311.1:p.Asp157IlefsTer26
NM_017841.4:c.469del MANE Select	NP_060311.1:p.Asp157IlefsTer26