Canonical Allele Identifier: CA2613848009

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446515-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446519del , CM000673.2:g.61446519del	GRCh38
NC_000011.9:g.61213991del , CM000673.1:g.61213991del	GRCh37
NC_000011.8:g.60970567del	NCBI36
NG_023393.1:g.21395del , LRG_519:g.21395del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*448del MANE Select	ENSP00000301761.3:n.*448del
ENST00000301761.6:c.*448del	ENSP00000301761.2:n.*448del
ENST00000536670.5:n.396+8406del
ENST00000538594.5:c.370+8406del	ENSP00000440939.1:n.370+8406del
ENST00000541135.5:c.377+8399del	ENSP00000443130.1:n.377+8399del
ENST00000542074.1:c.*528del	ENSP00000469670.1:n.*528del
ENST00000543044.2:c.*160+288del	ENSP00000440219.1:n.*160+288del
ENST00000544025.5:n.465+8406del
ENST00000544801.5:c.370+8406del	ENSP00000442581.1:n.370+8406del
ENST00000544880.1:n.374+8406del
NM_017841.2:c.*448del , LRG_519t1:c.*448del	NP_060311.1:n.*448del
NM_017841.4:c.*448del MANE Select	NP_060311.1:n.*448del