Canonical Allele Identifier: CA2613848051

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446529-CTGGTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446533_61446537del , CM000673.2:g.61446533_61446537del	GRCh38
NC_000011.9:g.61214005_61214009del , CM000673.1:g.61214005_61214009del	GRCh37
NC_000011.8:g.60970581_60970585del	NCBI36
NG_023393.1:g.21409_21413del , LRG_519:g.21409_21413del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*462_*466del MANE Select	ENSP00000301761.3:n.*462_*466del
ENST00000301761.6:c.*462_*466del	ENSP00000301761.2:n.*462_*466del
ENST00000536670.5:n.396+8420_396+8424del
ENST00000538594.5:c.370+8420_370+8424del	ENSP00000440939.1:n.370+8420_370+8424del
ENST00000541135.5:c.377+8413_377+8417del	ENSP00000443130.1:n.377+8413_377+8417del
ENST00000542074.1:c.*542_*546del	ENSP00000469670.1:n.*542_*546del
ENST00000543044.2:c.*160+302_*160+306del	ENSP00000440219.1:n.*160+302_*160+306del
ENST00000544025.5:n.465+8420_465+8424del
ENST00000544801.5:c.370+8420_370+8424del	ENSP00000442581.1:n.370+8420_370+8424del
ENST00000544880.1:n.374+8420_374+8424del
NM_017841.2:c.*462_*466del , LRG_519t1:c.*462_*466del	NP_060311.1:n.*462_*466del
NM_017841.4:c.*462_*466del MANE Select	NP_060311.1:n.*462_*466del