Canonical Allele Identifier: CA678946355

Gene: SDHAF2

Linked Data

• dbSNP Id: rs1291964611
• gnomAD v3: 11-61446134-TTA-T
• gnomAD v4: 11-61446134-TTA-T
• MyVariant Identifiers: chr11:g.61213607_61213608del (hg19) ; chr11:g.61446135_61446136del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446135_61446136del , CM000673.2:g.61446135_61446136del	GRCh38
NC_000011.9:g.61213607_61213608del , CM000673.1:g.61213607_61213608del	GRCh37
NC_000011.8:g.60970183_60970184del	NCBI36
NG_023393.1:g.21011_21012del , LRG_519:g.21011_21012del

Transcript Alleles

HGVS	Amino-acid change
ENST00000301761.7:c.*64_*65del MANE Select	ENSP00000301761.3:n.*64_*65del
ENST00000301761.6:c.*64_*65del	ENSP00000301761.2:n.*64_*65del
ENST00000536670.5:n.396+8022_396+8023del
ENST00000538594.5:c.370+8022_370+8023del	ENSP00000440939.1:n.370+8022_370+8023del
ENST00000541135.5:c.377+8015_377+8016del	ENSP00000443130.1:n.377+8015_377+8016del
ENST00000542074.1:c.*144_*145del	ENSP00000469670.1:n.*144_*145del
ENST00000542794.5:c.*567_*568del	ENSP00000439983.1:n.*567_*568del
ENST00000543044.2:c.*64_*65del	ENSP00000440219.1:n.*64_*65del
ENST00000544025.5:n.465+8022_465+8023del
ENST00000544801.5:c.370+8022_370+8023del	ENSP00000442581.1:n.370+8022_370+8023del
ENST00000544880.1:n.374+8022_374+8023del
NM_017841.2:c.*64_*65del , LRG_519t1:c.*64_*65del	NP_060311.1:n.*64_*65del
NM_017841.4:c.*64_*65del MANE Select	NP_060311.1:n.*64_*65del