Canonical Allele Identifier: CA2613847894

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446465-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446468del , CM000673.2:g.61446468del	GRCh38
NC_000011.9:g.61213940del , CM000673.1:g.61213940del	GRCh37
NC_000011.8:g.60970516del	NCBI36
NG_023393.1:g.21344del , LRG_519:g.21344del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*397del MANE Select	ENSP00000301761.3:n.*397del
ENST00000301761.6:c.*397del	ENSP00000301761.2:n.*397del
ENST00000536670.5:n.396+8355del
ENST00000538594.5:c.370+8355del	ENSP00000440939.1:n.370+8355del
ENST00000541135.5:c.377+8348del	ENSP00000443130.1:n.377+8348del
ENST00000542074.1:c.*477del	ENSP00000469670.1:n.*477del
ENST00000543044.2:c.*160+237del	ENSP00000440219.1:n.*160+237del
ENST00000544025.5:n.465+8355del
ENST00000544801.5:c.370+8355del	ENSP00000442581.1:n.370+8355del
ENST00000544880.1:n.374+8355del
NM_017841.2:c.*397del , LRG_519t1:c.*397del	NP_060311.1:n.*397del
NM_017841.4:c.*397del MANE Select	NP_060311.1:n.*397del