Canonical Allele Identifier: CA2724059351

Gene: SDHAF2

Linked Data

• dbSNP Id: rs2134902704

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446469_61446475del , CM000673.2:g.61446469_61446475del	GRCh38
NC_000011.9:g.61213941_61213947del , CM000673.1:g.61213941_61213947del	GRCh37
NC_000011.8:g.60970517_60970523del	NCBI36
NG_023393.1:g.21345_21351del , LRG_519:g.21345_21351del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*398_*404del MANE Select	ENSP00000301761.3:n.*398_*404del
ENST00000301761.6:c.*398_*404del	ENSP00000301761.2:n.*398_*404del
ENST00000536670.5:n.396+8356_396+8362del
ENST00000538594.5:c.370+8356_370+8362del	ENSP00000440939.1:n.370+8356_370+8362del
ENST00000541135.5:c.377+8349_377+8355del	ENSP00000443130.1:n.377+8349_377+8355del
ENST00000542074.1:c.*478_*484del	ENSP00000469670.1:n.*478_*484del
ENST00000543044.2:c.*160+238_*160+244del	ENSP00000440219.1:n.*160+238_*160+244del
ENST00000544025.5:n.465+8356_465+8362del
ENST00000544801.5:c.370+8356_370+8362del	ENSP00000442581.1:n.370+8356_370+8362del
ENST00000544880.1:n.374+8356_374+8362del
NM_017841.2:c.*398_*404del , LRG_519t1:c.*398_*404del	NP_060311.1:n.*398_*404del
NM_017841.4:c.*398_*404del MANE Select	NP_060311.1:n.*398_*404del