Canonical Allele Identifier: CA1977301541

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446456_61446457delinsCT , CM000673.2:g.61446456_61446457delinsCT	GRCh38
NC_000011.9:g.61213928_61213929delinsCT , CM000673.1:g.61213928_61213929delinsCT	GRCh37
NC_000011.8:g.60970504_60970505delinsCT	NCBI36
NG_023393.1:g.21332_21333delinsCT , LRG_519:g.21332_21333delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*385_*386delinsCT MANE Select	ENSP00000301761.3:n.*385_*386delinsCT
ENST00000301761.6:c.*385_*386delinsCT	ENSP00000301761.2:n.*385_*386delinsCT
ENST00000536670.5:n.396+8343_396+8344delinsCT
ENST00000538594.5:c.370+8343_370+8344delinsCT	ENSP00000440939.1:n.370+8343_370+8344delinsCT
ENST00000541135.5:c.377+8336_377+8337delinsCT	ENSP00000443130.1:n.377+8336_377+8337delinsCT
ENST00000542074.1:c.*465_*466delinsCT	ENSP00000469670.1:n.*465_*466delinsCT
ENST00000543044.2:c.*160+225_*160+226delinsCT	ENSP00000440219.1:n.*160+225_*160+226delinsCT
ENST00000544025.5:n.465+8343_465+8344delinsCT
ENST00000544801.5:c.370+8343_370+8344delinsCT	ENSP00000442581.1:n.370+8343_370+8344delinsCT
ENST00000544880.1:n.374+8343_374+8344delinsCT
NM_017841.2:c.*385_*386delinsCT , LRG_519t1:c.*385_*386delinsCT	NP_060311.1:n.*385_*386delinsCT
NM_017841.4:c.*385_*386delinsCT MANE Select	NP_060311.1:n.*385_*386delinsCT