Canonical Allele Identifier: CA2613847882

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446462-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446462C>G , CM000673.2:g.61446462C>G	GRCh38
NC_000011.9:g.61213934C>G , CM000673.1:g.61213934C>G	GRCh37
NC_000011.8:g.60970510C>G	NCBI36
NG_023393.1:g.21338C>G , LRG_519:g.21338C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*391C>G MANE Select	ENSP00000301761.3:n.*391C>G
ENST00000301761.6:c.*391C>G	ENSP00000301761.2:n.*391C>G
ENST00000536670.5:n.396+8349C>G
ENST00000538594.5:c.370+8349C>G	ENSP00000440939.1:n.370+8349C>G
ENST00000541135.5:c.377+8342C>G	ENSP00000443130.1:n.377+8342C>G
ENST00000542074.1:c.*471C>G	ENSP00000469670.1:n.*471C>G
ENST00000543044.2:c.*160+231C>G	ENSP00000440219.1:n.*160+231C>G
ENST00000544025.5:n.465+8349C>G
ENST00000544801.5:c.370+8349C>G	ENSP00000442581.1:n.370+8349C>G
ENST00000544880.1:n.374+8349C>G
NM_017841.2:c.*391C>G , LRG_519t1:c.*391C>G	NP_060311.1:n.*391C>G
NM_017841.4:c.*391C>G MANE Select	NP_060311.1:n.*391C>G