Canonical Allele Identifier: CA474523608

Gene: SDHAF2

Linked Data

• MyVariant Identifiers: chr11:g.61213534G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446062G>A , CM000673.2:g.61446062G>A	GRCh38
NC_000011.9:g.61213534G>A , CM000673.1:g.61213534G>A	GRCh37
NC_000011.8:g.60970110G>A	NCBI36
NG_023393.1:g.20938G>A , LRG_519:g.20938G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.492G>A MANE Select	ENSP00000301761.3:p.Lys164=
ENST00000301761.6:c.492G>A	ENSP00000301761.2:p.Lys164=
ENST00000536670.5:n.396+7949G>A
ENST00000538594.5:c.370+7949G>A	ENSP00000440939.1:n.370+7949G>A
ENST00000541135.5:c.377+7942G>A	ENSP00000443130.1:n.377+7942G>A
ENST00000542074.1:c.*71G>A	ENSP00000469670.1:n.*71G>A
ENST00000542794.5:c.*494G>A	ENSP00000439983.1:n.*494G>A
ENST00000543044.2:c.456G>A	ENSP00000440219.1:p.Lys152=
ENST00000543265.1:c.*115G>A	ENSP00000443660.1:n.*115G>A
ENST00000544025.5:n.465+7949G>A
ENST00000544801.5:c.370+7949G>A	ENSP00000442581.1:n.370+7949G>A
ENST00000544880.1:n.374+7949G>A
NM_017841.2:c.492G>A , LRG_519t1:c.492G>A	NP_060311.1:p.Lys164=
NM_017841.4:c.492G>A MANE Select	NP_060311.1:p.Lys164=