Canonical Allele Identifier: CA222882155

Gene: SDHAF2

Linked Data

• dbSNP Id: rs566595116
• gnomAD v2: 11-61213152-TCTG-T
• gnomAD v3: 11-61445680-TCTG-T
• gnomAD v4: 11-61445680-TCTG-T
• MyVariant Identifiers: chr11:g.61213153_61213155del (hg19) ; chr11:g.61445681_61445683del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61445684_61445686del , CM000673.2:g.61445684_61445686del	GRCh38
NC_000011.9:g.61213156_61213158del , CM000673.1:g.61213156_61213158del	GRCh37
NC_000011.8:g.60969732_60969734del	NCBI36
NG_023393.1:g.20560_20562del , LRG_519:g.20560_20562del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.371-257_371-255del MANE Select	ENSP00000301761.3:n.371-257_371-255del
ENST00000301761.6:c.371-257_371-255del	ENSP00000301761.2:n.371-257_371-255del
ENST00000359614.9:c.*79-257_*79-255del	ENSP00000352630.5:n.*79-257_*79-255del
ENST00000536670.5:n.396+7571_396+7573del
ENST00000537782.5:c.*17-257_*17-255del	ENSP00000469951.1:n.*17-257_*17-255del
ENST00000538594.5:c.370+7571_370+7573del	ENSP00000440939.1:n.370+7571_370+7573del
ENST00000541135.5:c.377+7564_377+7566del	ENSP00000443130.1:n.377+7564_377+7566del
ENST00000542074.1:c.37-257_37-255del	ENSP00000469670.1:n.37-257_37-255del
ENST00000542794.5:c.*373-257_*373-255del	ENSP00000439983.1:n.*373-257_*373-255del
ENST00000543044.2:c.335-257_335-255del	ENSP00000440219.1:n.335-257_335-255del
ENST00000543265.1:c.261-257_261-255del	ENSP00000443660.1:n.261-257_261-255del
ENST00000544025.5:n.465+7571_465+7573del
ENST00000544801.5:c.370+7571_370+7573del	ENSP00000442581.1:n.370+7571_370+7573del
ENST00000544880.1:n.374+7571_374+7573del
NM_017841.2:c.371-257_371-255del , LRG_519t1:c.371-257_371-255del	NP_060311.1:n.371-257_371-255del
NM_017841.4:c.371-257_371-255del MANE Select	NP_060311.1:n.371-257_371-255del