Canonical Allele Identifier: CA1977293883
Gene: SDHAF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61437973C= , CM000673.2:g.61437973C= GRCh38
NC_000011.9:g.61205445C= , CM000673.1:g.61205445C= GRCh37
NC_000011.8:g.60962021C= NCBI36
NG_023393.1:g.12849C= , LRG_519:g.12849C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.261-31C= MANE Select ENSP00000301761.3:n.261-31C=
ENST00000301761.6:c.261-31C= ENSP00000301761.2:n.261-31C=
ENST00000359614.9:c.261-31C= ENSP00000352630.5:n.261-31C=
ENST00000534878.5:c.261-31C= ENSP00000471030.1:n.261-31C=
ENST00000536250.1:c.*263-31C= ENSP00000471120.1:n.*263-31C=
ENST00000536670.5:n.287-31C=
ENST00000537782.5:c.261-31C= ENSP00000469951.1:n.261-31C=
ENST00000538594.5:c.261-31C= ENSP00000440939.1:n.261-31C=
ENST00000541135.5:c.261-31C= ENSP00000443130.1:n.261-31C=
ENST00000542074.1:c.36+7791C= ENSP00000469670.1:n.36+7791C=
ENST00000542794.5:c.*263-31C= ENSP00000439983.1:n.*263-31C=
ENST00000543044.2:c.225-31C= ENSP00000440219.1:n.225-31C=
ENST00000543265.1:c.260+125C= ENSP00000443660.1:n.260+125C=
ENST00000544025.5:n.356-31C=
ENST00000544801.5:c.261-31C= ENSP00000442581.1:n.261-31C=
ENST00000544880.1:n.265-31C=
NM_017841.2:c.261-31C= , LRG_519t1:c.261-31C= NP_060311.1:n.261-31C=
NM_017841.4:c.261-31C= MANE Select NP_060311.1:n.261-31C=