Canonical Allele Identifier: CA2574841570

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446096-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446096G>C , CM000673.2:g.61446096G>C	GRCh38
NC_000011.9:g.61213568G>C , CM000673.1:g.61213568G>C	GRCh37
NC_000011.8:g.60970144G>C	NCBI36
NG_023393.1:g.20972G>C , LRG_519:g.20972G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000301761.7:c.*25G>C MANE Select	ENSP00000301761.3:n.*25G>C
ENST00000301761.6:c.*25G>C	ENSP00000301761.2:n.*25G>C
ENST00000536670.5:n.396+7983G>C
ENST00000538594.5:c.370+7983G>C	ENSP00000440939.1:n.370+7983G>C
ENST00000541135.5:c.377+7976G>C	ENSP00000443130.1:n.377+7976G>C
ENST00000542074.1:c.*105G>C	ENSP00000469670.1:n.*105G>C
ENST00000542794.5:c.*528G>C	ENSP00000439983.1:n.*528G>C
ENST00000543044.2:c.*25G>C	ENSP00000440219.1:n.*25G>C
ENST00000543265.1:c.*149G>C	ENSP00000443660.1:n.*149G>C
ENST00000544025.5:n.465+7983G>C
ENST00000544801.5:c.370+7983G>C	ENSP00000442581.1:n.370+7983G>C
ENST00000544880.1:n.374+7983G>C
NM_017841.2:c.*25G>C , LRG_519t1:c.*25G>C	NP_060311.1:n.*25G>C
NM_017841.4:c.*25G>C MANE Select	NP_060311.1:n.*25G>C