Canonical Allele Identifier: CA599504172

Gene: SDHAF2

Linked Data

• dbSNP Id: rs1464132517
• gnomAD v2: 11-61213866-TGCCTCA-T
• gnomAD v3: 11-61446394-TGCCTCA-T
• gnomAD v4: 11-61446394-TGCCTCA-T
• MyVariant Identifiers: chr11:g.61213867_61213872del (hg19) ; chr11:g.61446395_61446400del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446398_61446403del , CM000673.2:g.61446398_61446403del	GRCh38
NC_000011.9:g.61213870_61213875del , CM000673.1:g.61213870_61213875del	GRCh37
NC_000011.8:g.60970446_60970451del	NCBI36
NG_023393.1:g.21274_21279del , LRG_519:g.21274_21279del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*327_*332del MANE Select	ENSP00000301761.3:n.*327_*332del
ENST00000301761.6:c.*327_*332del	ENSP00000301761.2:n.*327_*332del
ENST00000536670.5:n.396+8285_396+8290del
ENST00000538594.5:c.370+8285_370+8290del	ENSP00000440939.1:n.370+8285_370+8290del
ENST00000541135.5:c.377+8278_377+8283del	ENSP00000443130.1:n.377+8278_377+8283del
ENST00000542074.1:c.*407_*412del	ENSP00000469670.1:n.*407_*412del
ENST00000543044.2:c.*160+167_*160+172del	ENSP00000440219.1:n.*160+167_*160+172del
ENST00000544025.5:n.465+8285_465+8290del
ENST00000544801.5:c.370+8285_370+8290del	ENSP00000442581.1:n.370+8285_370+8290del
ENST00000544880.1:n.374+8285_374+8290del
NM_017841.2:c.*327_*332del , LRG_519t1:c.*327_*332del	NP_060311.1:n.*327_*332del
NM_017841.4:c.*327_*332del MANE Select	NP_060311.1:n.*327_*332del