Canonical Allele Identifier: CA2613847872

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446457-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446460del , CM000673.2:g.61446460del	GRCh38
NC_000011.9:g.61213932del , CM000673.1:g.61213932del	GRCh37
NC_000011.8:g.60970508del	NCBI36
NG_023393.1:g.21336del , LRG_519:g.21336del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*389del MANE Select	ENSP00000301761.3:n.*389del
ENST00000301761.6:c.*389del	ENSP00000301761.2:n.*389del
ENST00000536670.5:n.396+8347del
ENST00000538594.5:c.370+8347del	ENSP00000440939.1:n.370+8347del
ENST00000541135.5:c.377+8340del	ENSP00000443130.1:n.377+8340del
ENST00000542074.1:c.*469del	ENSP00000469670.1:n.*469del
ENST00000543044.2:c.*160+229del	ENSP00000440219.1:n.*160+229del
ENST00000544025.5:n.465+8347del
ENST00000544801.5:c.370+8347del	ENSP00000442581.1:n.370+8347del
ENST00000544880.1:n.374+8347del
NM_017841.2:c.*389del , LRG_519t1:c.*389del	NP_060311.1:n.*389del
NM_017841.4:c.*389del MANE Select	NP_060311.1:n.*389del