Canonical Allele Identifier: CA1977300697
Gene: SDHAF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61445756A= , CM000673.2:g.61445756A= GRCh38
NC_000011.9:g.61213228A= , CM000673.1:g.61213228A= GRCh37
NC_000011.8:g.60969804A= NCBI36
NG_023393.1:g.20632A= , LRG_519:g.20632A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.371-185A= MANE Select ENSP00000301761.3:n.371-185A=
ENST00000301761.6:c.371-185A= ENSP00000301761.2:n.371-185A=
ENST00000359614.9:c.*79-185A= ENSP00000352630.5:n.*79-185A=
ENST00000536670.5:n.396+7643A=
ENST00000537782.5:c.*17-185A= ENSP00000469951.1:n.*17-185A=
ENST00000538594.5:c.370+7643A= ENSP00000440939.1:n.370+7643A=
ENST00000541135.5:c.377+7636A= ENSP00000443130.1:n.377+7636A=
ENST00000542074.1:c.37-185A= ENSP00000469670.1:n.37-185A=
ENST00000542794.5:c.*373-185A= ENSP00000439983.1:n.*373-185A=
ENST00000543044.2:c.335-185A= ENSP00000440219.1:n.335-185A=
ENST00000543265.1:c.261-185A= ENSP00000443660.1:n.261-185A=
ENST00000544025.5:n.465+7643A=
ENST00000544801.5:c.370+7643A= ENSP00000442581.1:n.370+7643A=
ENST00000544880.1:n.374+7643A=
NM_017841.2:c.371-185A= , LRG_519t1:c.371-185A= NP_060311.1:n.371-185A=
NM_017841.4:c.371-185A= MANE Select NP_060311.1:n.371-185A=