Canonical Allele Identifier: CA2613847639

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446261-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446261_61446262insG , CM000673.2:g.61446261_61446262insG	GRCh38
NC_000011.9:g.61213733_61213734insG , CM000673.1:g.61213733_61213734insG	GRCh37
NC_000011.8:g.60970309_60970310insG	NCBI36
NG_023393.1:g.21137_21138insG , LRG_519:g.21137_21138insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*190_*191insG MANE Select	ENSP00000301761.3:n.*190_*191insG
ENST00000301761.6:c.*190_*191insG	ENSP00000301761.2:n.*190_*191insG
ENST00000536670.5:n.396+8148_396+8149insG
ENST00000538594.5:c.370+8148_370+8149insG	ENSP00000440939.1:n.370+8148_370+8149insG
ENST00000541135.5:c.377+8141_377+8142insG	ENSP00000443130.1:n.377+8141_377+8142insG
ENST00000542074.1:c.*270_*271insG	ENSP00000469670.1:n.*270_*271insG
ENST00000542794.5:c.*693_*694insG	ENSP00000439983.1:n.*693_*694insG
ENST00000543044.2:c.*160+30_*160+31insG	ENSP00000440219.1:n.*160+30_*160+31insG
ENST00000544025.5:n.465+8148_465+8149insG
ENST00000544801.5:c.370+8148_370+8149insG	ENSP00000442581.1:n.370+8148_370+8149insG
ENST00000544880.1:n.374+8148_374+8149insG
NM_017841.2:c.*190_*191insG , LRG_519t1:c.*190_*191insG	NP_060311.1:n.*190_*191insG
NM_017841.4:c.*190_*191insG MANE Select	NP_060311.1:n.*190_*191insG