Canonical Allele Identifier: CA474523462

Gene: SDHAF2

Linked Data

• MyVariant Identifiers: chr11:g.61213474T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446002T>A , CM000673.2:g.61446002T>A	GRCh38
NC_000011.9:g.61213474T>A , CM000673.1:g.61213474T>A	GRCh37
NC_000011.8:g.60970050T>A	NCBI36
NG_023393.1:g.20878T>A , LRG_519:g.20878T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.432T>A MANE Select	ENSP00000301761.3:p.Ala144=
ENST00000301761.6:c.432T>A	ENSP00000301761.2:p.Ala144=
ENST00000359614.9:c.*140T>A	ENSP00000352630.5:n.*140T>A
ENST00000536670.5:n.396+7889T>A
ENST00000537782.5:c.*78T>A	ENSP00000469951.1:n.*78T>A
ENST00000538594.5:c.370+7889T>A	ENSP00000440939.1:n.370+7889T>A
ENST00000541135.5:c.377+7882T>A	ENSP00000443130.1:n.377+7882T>A
ENST00000542074.1:c.*11T>A	ENSP00000469670.1:n.*11T>A
ENST00000542794.5:c.*434T>A	ENSP00000439983.1:n.*434T>A
ENST00000543044.2:c.396T>A	ENSP00000440219.1:p.Ala132=
ENST00000543265.1:c.*55T>A	ENSP00000443660.1:n.*55T>A
ENST00000544025.5:n.465+7889T>A
ENST00000544801.5:c.370+7889T>A	ENSP00000442581.1:n.370+7889T>A
ENST00000544880.1:n.374+7889T>A
NM_017841.2:c.432T>A , LRG_519t1:c.432T>A	NP_060311.1:p.Ala144=
NM_017841.4:c.432T>A MANE Select	NP_060311.1:p.Ala144=