Canonical Allele Identifier: CA2613847873

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446457-TCCCGCCCTCCCTGCAGCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446467_61446485del , CM000673.2:g.61446467_61446485del	GRCh38
NC_000011.9:g.61213939_61213957del , CM000673.1:g.61213939_61213957del	GRCh37
NC_000011.8:g.60970515_60970533del	NCBI36
NG_023393.1:g.21343_21361del , LRG_519:g.21343_21361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*396_*414del MANE Select	ENSP00000301761.3:n.*396_*414del
ENST00000301761.6:c.*396_*414del	ENSP00000301761.2:n.*396_*414del
ENST00000536670.5:n.396+8354_396+8372del
ENST00000538594.5:c.370+8354_370+8372del	ENSP00000440939.1:n.370+8354_370+8372del
ENST00000541135.5:c.377+8347_377+8365del	ENSP00000443130.1:n.377+8347_377+8365del
ENST00000542074.1:c.*476_*494del	ENSP00000469670.1:n.*476_*494del
ENST00000543044.2:c.*160+236_*160+254del	ENSP00000440219.1:n.*160+236_*160+254del
ENST00000544025.5:n.465+8354_465+8372del
ENST00000544801.5:c.370+8354_370+8372del	ENSP00000442581.1:n.370+8354_370+8372del
ENST00000544880.1:n.374+8354_374+8372del
NM_017841.2:c.*396_*414del , LRG_519t1:c.*396_*414del	NP_060311.1:n.*396_*414del
NM_017841.4:c.*396_*414del MANE Select	NP_060311.1:n.*396_*414del