Canonical Allele Identifier: CA380685485

Gene: SDHAF2

Linked Data

• MyVariant Identifiers: chr11:g.61213506C>G (hg19) ; chr11:g.61446034C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446034C>G , CM000673.2:g.61446034C>G	GRCh38
NC_000011.9:g.61213506C>G , CM000673.1:g.61213506C>G	GRCh37
NC_000011.8:g.60970082C>G	NCBI36
NG_023393.1:g.20910C>G , LRG_519:g.20910C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.464C>G MANE Select	ENSP00000301761.3:p.Ala155Gly
ENST00000301761.6:c.464C>G	ENSP00000301761.2:p.Ala155Gly
ENST00000536670.5:n.396+7921C>G
ENST00000537782.5:c.*110C>G	ENSP00000469951.1:n.*110C>G
ENST00000538594.5:c.370+7921C>G	ENSP00000440939.1:n.370+7921C>G
ENST00000541135.5:c.377+7914C>G	ENSP00000443130.1:n.377+7914C>G
ENST00000542074.1:c.*43C>G	ENSP00000469670.1:n.*43C>G
ENST00000542794.5:c.*466C>G	ENSP00000439983.1:n.*466C>G
ENST00000543044.2:c.428C>G	ENSP00000440219.1:p.Ala143Gly
ENST00000543265.1:c.*87C>G	ENSP00000443660.1:n.*87C>G
ENST00000544025.5:n.465+7921C>G
ENST00000544801.5:c.370+7921C>G	ENSP00000442581.1:n.370+7921C>G
ENST00000544880.1:n.374+7921C>G
NM_017841.2:c.464C>G , LRG_519t1:c.464C>G	NP_060311.1:p.Ala155Gly
NM_017841.4:c.464C>G MANE Select	NP_060311.1:p.Ala155Gly