Canonical Allele Identifier: CA2613847807

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446420-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446420_61446421insT , CM000673.2:g.61446420_61446421insT	GRCh38
NC_000011.9:g.61213892_61213893insT , CM000673.1:g.61213892_61213893insT	GRCh37
NC_000011.8:g.60970468_60970469insT	NCBI36
NG_023393.1:g.21296_21297insT , LRG_519:g.21296_21297insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*349_*350insT MANE Select	ENSP00000301761.3:n.*349_*350insT
ENST00000301761.6:c.*349_*350insT	ENSP00000301761.2:n.*349_*350insT
ENST00000536670.5:n.396+8307_396+8308insT
ENST00000538594.5:c.370+8307_370+8308insT	ENSP00000440939.1:n.370+8307_370+8308insT
ENST00000541135.5:c.377+8300_377+8301insT	ENSP00000443130.1:n.377+8300_377+8301insT
ENST00000542074.1:c.*429_*430insT	ENSP00000469670.1:n.*429_*430insT
ENST00000543044.2:c.*160+189_*160+190insT	ENSP00000440219.1:n.*160+189_*160+190insT
ENST00000544025.5:n.465+8307_465+8308insT
ENST00000544801.5:c.370+8307_370+8308insT	ENSP00000442581.1:n.370+8307_370+8308insT
ENST00000544880.1:n.374+8307_374+8308insT
NM_017841.2:c.*349_*350insT , LRG_519t1:c.*349_*350insT	NP_060311.1:n.*349_*350insT
NM_017841.4:c.*349_*350insT MANE Select	NP_060311.1:n.*349_*350insT