Canonical Allele Identifier: CA474523547

Gene: SDHAF2

Linked Data

• MyVariant Identifiers: chr11:g.61213507C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446035C>G , CM000673.2:g.61446035C>G	GRCh38
NC_000011.9:g.61213507C>G , CM000673.1:g.61213507C>G	GRCh37
NC_000011.8:g.60970083C>G	NCBI36
NG_023393.1:g.20911C>G , LRG_519:g.20911C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.465C>G MANE Select	ENSP00000301761.3:p.Ala155=
ENST00000301761.6:c.465C>G	ENSP00000301761.2:p.Ala155=
ENST00000536670.5:n.396+7922C>G
ENST00000537782.5:c.*111C>G	ENSP00000469951.1:n.*111C>G
ENST00000538594.5:c.370+7922C>G	ENSP00000440939.1:n.370+7922C>G
ENST00000541135.5:c.377+7915C>G	ENSP00000443130.1:n.377+7915C>G
ENST00000542074.1:c.*44C>G	ENSP00000469670.1:n.*44C>G
ENST00000542794.5:c.*467C>G	ENSP00000439983.1:n.*467C>G
ENST00000543044.2:c.429C>G	ENSP00000440219.1:p.Ala143=
ENST00000543265.1:c.*88C>G	ENSP00000443660.1:n.*88C>G
ENST00000544025.5:n.465+7922C>G
ENST00000544801.5:c.370+7922C>G	ENSP00000442581.1:n.370+7922C>G
ENST00000544880.1:n.374+7922C>G
NM_017841.2:c.465C>G , LRG_519t1:c.465C>G	NP_060311.1:p.Ala155=
NM_017841.4:c.465C>G MANE Select	NP_060311.1:p.Ala155=