Canonical Allele Identifier: CA474523530

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446029-G-T
• MyVariant Identifiers: chr11:g.61213501G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446029G>T , CM000673.2:g.61446029G>T	GRCh38
NC_000011.9:g.61213501G>T , CM000673.1:g.61213501G>T	GRCh37
NC_000011.8:g.60970077G>T	NCBI36
NG_023393.1:g.20905G>T , LRG_519:g.20905G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.459G>T MANE Select	ENSP00000301761.3:p.Leu153=
ENST00000301761.6:c.459G>T	ENSP00000301761.2:p.Leu153=
ENST00000536670.5:n.396+7916G>T
ENST00000537782.5:c.*105G>T	ENSP00000469951.1:n.*105G>T
ENST00000538594.5:c.370+7916G>T	ENSP00000440939.1:n.370+7916G>T
ENST00000541135.5:c.377+7909G>T	ENSP00000443130.1:n.377+7909G>T
ENST00000542074.1:c.*38G>T	ENSP00000469670.1:n.*38G>T
ENST00000542794.5:c.*461G>T	ENSP00000439983.1:n.*461G>T
ENST00000543044.2:c.423G>T	ENSP00000440219.1:p.Leu141=
ENST00000543265.1:c.*82G>T	ENSP00000443660.1:n.*82G>T
ENST00000544025.5:n.465+7916G>T
ENST00000544801.5:c.370+7916G>T	ENSP00000442581.1:n.370+7916G>T
ENST00000544880.1:n.374+7916G>T
NM_017841.2:c.459G>T , LRG_519t1:c.459G>T	NP_060311.1:p.Leu153=
NM_017841.4:c.459G>T MANE Select	NP_060311.1:p.Leu153=