Canonical Allele Identifier: CA380685699

Gene: SDHAF2

Linked Data

• MyVariant Identifiers: chr11:g.61213542G>C (hg19) ; chr11:g.61446070G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446070G>C , CM000673.2:g.61446070G>C	GRCh38
NC_000011.9:g.61213542G>C , CM000673.1:g.61213542G>C	GRCh37
NC_000011.8:g.60970118G>C	NCBI36
NG_023393.1:g.20946G>C , LRG_519:g.20946G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.500G>C MANE Select	ENSP00000301761.3:p.Ter167Ser
ENST00000301761.6:c.500G>C	ENSP00000301761.2:p.Ter167Ser
ENST00000536670.5:n.396+7957G>C
ENST00000538594.5:c.370+7957G>C	ENSP00000440939.1:n.370+7957G>C
ENST00000541135.5:c.377+7950G>C	ENSP00000443130.1:n.377+7950G>C
ENST00000542074.1:c.*79G>C	ENSP00000469670.1:n.*79G>C
ENST00000542794.5:c.*502G>C	ENSP00000439983.1:n.*502G>C
ENST00000543044.2:c.464G>C	ENSP00000440219.1:p.Ter155Ser
ENST00000543265.1:c.*123G>C	ENSP00000443660.1:n.*123G>C
ENST00000544025.5:n.465+7957G>C
ENST00000544801.5:c.370+7957G>C	ENSP00000442581.1:n.370+7957G>C
ENST00000544880.1:n.374+7957G>C
NM_017841.2:c.500G>C , LRG_519t1:c.500G>C	NP_060311.1:p.Ter167Ser
NM_017841.4:c.500G>C MANE Select	NP_060311.1:p.Ter167Ser