Canonical Allele Identifier: CA2613847959

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446495-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446495G>T , CM000673.2:g.61446495G>T	GRCh38
NC_000011.9:g.61213967G>T , CM000673.1:g.61213967G>T	GRCh37
NC_000011.8:g.60970543G>T	NCBI36
NG_023393.1:g.21371G>T , LRG_519:g.21371G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*424G>T MANE Select	ENSP00000301761.3:n.*424G>T
ENST00000301761.6:c.*424G>T	ENSP00000301761.2:n.*424G>T
ENST00000536670.5:n.396+8382G>T
ENST00000538594.5:c.370+8382G>T	ENSP00000440939.1:n.370+8382G>T
ENST00000541135.5:c.377+8375G>T	ENSP00000443130.1:n.377+8375G>T
ENST00000542074.1:c.*504G>T	ENSP00000469670.1:n.*504G>T
ENST00000543044.2:c.*160+264G>T	ENSP00000440219.1:n.*160+264G>T
ENST00000544025.5:n.465+8382G>T
ENST00000544801.5:c.370+8382G>T	ENSP00000442581.1:n.370+8382G>T
ENST00000544880.1:n.374+8382G>T
NM_017841.2:c.*424G>T , LRG_519t1:c.*424G>T	NP_060311.1:n.*424G>T
NM_017841.4:c.*424G>T MANE Select	NP_060311.1:n.*424G>T