Canonical Allele Identifier: CA380685229

Gene: SDHAF2

Linked Data

• MyVariant Identifiers: chr11:g.61213417T>A (hg19) ; chr11:g.61445945T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61445945T>A , CM000673.2:g.61445945T>A	GRCh38
NC_000011.9:g.61213417T>A , CM000673.1:g.61213417T>A	GRCh37
NC_000011.8:g.60969993T>A	NCBI36
NG_023393.1:g.20821T>A , LRG_519:g.20821T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.375T>A MANE Select	ENSP00000301761.3:p.Ala125=
ENST00000301761.6:c.375T>A	ENSP00000301761.2:p.Ala125=
ENST00000359614.9:c.*83T>A	ENSP00000352630.5:n.*83T>A
ENST00000536670.5:n.396+7832T>A
ENST00000537782.5:c.*21T>A	ENSP00000469951.1:n.*21T>A
ENST00000538594.5:c.370+7832T>A	ENSP00000440939.1:n.370+7832T>A
ENST00000541135.5:c.377+7825T>A	ENSP00000443130.1:n.377+7825T>A
ENST00000542074.1:c.41T>A	ENSP00000469670.1:p.Leu14Gln
ENST00000542794.5:c.*377T>A	ENSP00000439983.1:n.*377T>A
ENST00000543044.2:c.339T>A	ENSP00000440219.1:p.Ala113=
ENST00000543265.1:c.265T>A	ENSP00000443660.1:p.Ter89Lys
ENST00000544025.5:n.465+7832T>A
ENST00000544801.5:c.370+7832T>A	ENSP00000442581.1:n.370+7832T>A
ENST00000544880.1:n.374+7832T>A
NM_017841.2:c.375T>A , LRG_519t1:c.375T>A	NP_060311.1:p.Ala125=
NM_017841.4:c.375T>A MANE Select	NP_060311.1:p.Ala125=