Canonical Allele Identifier: CA2613848000

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446513-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446513A>T , CM000673.2:g.61446513A>T	GRCh38
NC_000011.9:g.61213985A>T , CM000673.1:g.61213985A>T	GRCh37
NC_000011.8:g.60970561A>T	NCBI36
NG_023393.1:g.21389A>T , LRG_519:g.21389A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*442A>T MANE Select	ENSP00000301761.3:n.*442A>T
ENST00000301761.6:c.*442A>T	ENSP00000301761.2:n.*442A>T
ENST00000536670.5:n.396+8400A>T
ENST00000538594.5:c.370+8400A>T	ENSP00000440939.1:n.370+8400A>T
ENST00000541135.5:c.377+8393A>T	ENSP00000443130.1:n.377+8393A>T
ENST00000542074.1:c.*522A>T	ENSP00000469670.1:n.*522A>T
ENST00000543044.2:c.*160+282A>T	ENSP00000440219.1:n.*160+282A>T
ENST00000544025.5:n.465+8400A>T
ENST00000544801.5:c.370+8400A>T	ENSP00000442581.1:n.370+8400A>T
ENST00000544880.1:n.374+8400A>T
NM_017841.2:c.*442A>T , LRG_519t1:c.*442A>T	NP_060311.1:n.*442A>T
NM_017841.4:c.*442A>T MANE Select	NP_060311.1:n.*442A>T