Canonical Allele Identifier: CA474523598

Gene: SDHAF2

Linked Data

• MyVariant Identifiers: chr11:g.61213525C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446053C>A , CM000673.2:g.61446053C>A	GRCh38
NC_000011.9:g.61213525C>A , CM000673.1:g.61213525C>A	GRCh37
NC_000011.8:g.60970101C>A	NCBI36
NG_023393.1:g.20929C>A , LRG_519:g.20929C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.483C>A MANE Select	ENSP00000301761.3:p.Leu161=
ENST00000301761.6:c.483C>A	ENSP00000301761.2:p.Leu161=
ENST00000536670.5:n.396+7940C>A
ENST00000537782.5:c.*129C>A	ENSP00000469951.1:n.*129C>A
ENST00000538594.5:c.370+7940C>A	ENSP00000440939.1:n.370+7940C>A
ENST00000541135.5:c.377+7933C>A	ENSP00000443130.1:n.377+7933C>A
ENST00000542074.1:c.*62C>A	ENSP00000469670.1:n.*62C>A
ENST00000542794.5:c.*485C>A	ENSP00000439983.1:n.*485C>A
ENST00000543044.2:c.447C>A	ENSP00000440219.1:p.Leu149=
ENST00000543265.1:c.*106C>A	ENSP00000443660.1:n.*106C>A
ENST00000544025.5:n.465+7940C>A
ENST00000544801.5:c.370+7940C>A	ENSP00000442581.1:n.370+7940C>A
ENST00000544880.1:n.374+7940C>A
NM_017841.2:c.483C>A , LRG_519t1:c.483C>A	NP_060311.1:p.Leu161=
NM_017841.4:c.483C>A MANE Select	NP_060311.1:p.Leu161=