Canonical Allele Identifier: CA654542491

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446092-A-G
• COSMIC: COSN1540002

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446092A>G , CM000673.2:g.61446092A>G	GRCh38
NC_000011.9:g.61213564A>G , CM000673.1:g.61213564A>G	GRCh37
NC_000011.8:g.60970140A>G	NCBI36
NG_023393.1:g.20968A>G , LRG_519:g.20968A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*21A>G MANE Select	ENSP00000301761.3:n.*21A>G
ENST00000301761.6:c.*21A>G	ENSP00000301761.2:n.*21A>G
ENST00000536670.5:n.396+7979A>G
ENST00000538594.5:c.370+7979A>G	ENSP00000440939.1:n.370+7979A>G
ENST00000541135.5:c.377+7972A>G	ENSP00000443130.1:n.377+7972A>G
ENST00000542074.1:c.*101A>G	ENSP00000469670.1:n.*101A>G
ENST00000542794.5:c.*524A>G	ENSP00000439983.1:n.*524A>G
ENST00000543044.2:c.*21A>G	ENSP00000440219.1:n.*21A>G
ENST00000543265.1:c.*145A>G	ENSP00000443660.1:n.*145A>G
ENST00000544025.5:n.465+7979A>G
ENST00000544801.5:c.370+7979A>G	ENSP00000442581.1:n.370+7979A>G
ENST00000544880.1:n.374+7979A>G
NM_017841.2:c.*21A>G , LRG_519t1:c.*21A>G	NP_060311.1:n.*21A>G
NM_017841.4:c.*21A>G MANE Select	NP_060311.1:n.*21A>G