Canonical Allele Identifier: CA2613847603
Gene: SDHAF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446241_61446242del , CM000673.2:g.61446241_61446242del GRCh38
NC_000011.9:g.61213713_61213714del , CM000673.1:g.61213713_61213714del GRCh37
NC_000011.8:g.60970289_60970290del NCBI36
NG_023393.1:g.21117_21118del , LRG_519:g.21117_21118del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.*170_*171del MANE Select ENSP00000301761.3:n.*170_*171del
ENST00000301761.6:c.*170_*171del ENSP00000301761.2:n.*170_*171del
ENST00000536670.5:n.396+8128_396+8129del
ENST00000538594.5:c.370+8128_370+8129del ENSP00000440939.1:n.370+8128_370+8129del
ENST00000541135.5:c.377+8121_377+8122del ENSP00000443130.1:n.377+8121_377+8122del
ENST00000542074.1:c.*250_*251del ENSP00000469670.1:n.*250_*251del
ENST00000542794.5:c.*673_*674del ENSP00000439983.1:n.*673_*674del
ENST00000543044.2:c.*160+10_*160+11del ENSP00000440219.1:n.*160+10_*160+11del
ENST00000544025.5:n.465+8128_465+8129del
ENST00000544801.5:c.370+8128_370+8129del ENSP00000442581.1:n.370+8128_370+8129del
ENST00000544880.1:n.374+8128_374+8129del
NM_017841.2:c.*170_*171del , LRG_519t1:c.*170_*171del NP_060311.1:n.*170_*171del
NM_017841.4:c.*170_*171del MANE Select NP_060311.1:n.*170_*171del