Canonical Allele Identifier: CA1977301549

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446457_61446502delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG , CM000673.2:g.61446457_61446502delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG	GRCh38
NC_000011.9:g.61213929_61213974delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG , CM000673.1:g.61213929_61213974delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG	GRCh37
NC_000011.8:g.60970505_60970550delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG	NCBI36
NG_023393.1:g.21333_21378delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG , LRG_519:g.21333_21378delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*386_*431delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG MANE Select	ENSP00000301761.3:n.*386_*431delinsTCCCGCCCTCCCTGCAGCTCCCCGCC...
ENST00000301761.6:c.*386_*431delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG	ENSP00000301761.2:n.*386_*431delinsTCCCGCCCTCCCTGCAGCTCCCCGCC...
ENST00000536670.5:n.396+8344_396+8389delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG
ENST00000538594.5:c.370+8344_370+8389delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG	ENSP00000440939.1:n.370+8344_370+8389delinsTCCCGCCCTCCCTGCAGC...
ENST00000541135.5:c.377+8337_377+8382delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG	ENSP00000443130.1:n.377+8337_377+8382delinsTCCCGCCCTCCCTGCAGC...
ENST00000542074.1:c.*466_*511delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG	ENSP00000469670.1:n.*466_*511delinsTCCCGCCCTCCCTGCAGCTCCCCGCC...
ENST00000543044.2:c.*160+226_*160+271delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG	ENSP00000440219.1:n.*160+226_*160+271delinsTCCCGCCCTCCCTGCAGC...
ENST00000544025.5:n.465+8344_465+8389delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG
ENST00000544801.5:c.370+8344_370+8389delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG	ENSP00000442581.1:n.370+8344_370+8389delinsTCCCGCCCTCCCTGCAGC...
ENST00000544880.1:n.374+8344_374+8389delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG
NM_017841.2:c.*386_*431delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG , LRG_519t1:c.*386_*431delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG	NP_060311.1:n.*386_*431delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGT...
NM_017841.4:c.*386_*431delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGTGGCCCAGGGCTTTG MANE Select	NP_060311.1:n.*386_*431delinsTCCCGCCCTCCCTGCAGCTCCCCGCCCTCAGT...