Canonical Allele Identifier: CA058257

Gene: SDHAF2

Linked Data

• dbSNP Id: rs536680634
• ExAC: 11:61205444 CCT / C
• gnomAD v4: 11-61437972-CCT-C
• MyVariant Identifiers: chr11:g.61205445_61205446del (hg19) ; chr11:g.61437973_61437974del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61437975_61437976del , CM000673.2:g.61437975_61437976del	GRCh38
NC_000011.9:g.61205447_61205448del , CM000673.1:g.61205447_61205448del	GRCh37
NC_000011.8:g.60962023_60962024del	NCBI36
NG_023393.1:g.12851_12852del , LRG_519:g.12851_12852del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.261-29_261-28del MANE Select	ENSP00000301761.3:n.261-29_261-28del
ENST00000301761.6:c.261-29_261-28del	ENSP00000301761.2:n.261-29_261-28del
ENST00000359614.9:c.261-29_261-28del	ENSP00000352630.5:n.261-29_261-28del
ENST00000534878.5:c.261-29_261-28del	ENSP00000471030.1:n.261-29_261-28del
ENST00000536250.1:c.*263-29_*263-28del	ENSP00000471120.1:n.*263-29_*263-28del
ENST00000536670.5:n.287-29_287-28del
ENST00000537782.5:c.261-29_261-28del	ENSP00000469951.1:n.261-29_261-28del
ENST00000538594.5:c.261-29_261-28del	ENSP00000440939.1:n.261-29_261-28del
ENST00000541135.5:c.261-29_261-28del	ENSP00000443130.1:n.261-29_261-28del
ENST00000542074.1:c.36+7793_36+7794del	ENSP00000469670.1:n.36+7793_36+7794del
ENST00000542794.5:c.*263-29_*263-28del	ENSP00000439983.1:n.*263-29_*263-28del
ENST00000543044.2:c.225-29_225-28del	ENSP00000440219.1:n.225-29_225-28del
ENST00000543265.1:c.260+127_260+128del	ENSP00000443660.1:n.260+127_260+128del
ENST00000544025.5:n.356-29_356-28del
ENST00000544801.5:c.261-29_261-28del	ENSP00000442581.1:n.261-29_261-28del
ENST00000544880.1:n.265-29_265-28del
NM_017841.2:c.261-29_261-28del , LRG_519t1:c.261-29_261-28del	NP_060311.1:n.261-29_261-28del
NM_017841.4:c.261-29_261-28del MANE Select	NP_060311.1:n.261-29_261-28del