Canonical Allele Identifier: CA474803018
Gene: SDHAF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.61205315T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61437843T>C , CM000673.2:g.61437843T>C GRCh38
NC_000011.9:g.61205315T>C , CM000673.1:g.61205315T>C GRCh37
NC_000011.8:g.60961891T>C NCBI36
NG_023393.1:g.12719T>C , LRG_519:g.12719T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.255T>C MANE Select ENSP00000301761.3:p.Leu85=
ENST00000301761.6:c.255T>C ENSP00000301761.2:p.Leu85=
ENST00000359614.9:c.255T>C ENSP00000352630.5:p.Leu85=
ENST00000534878.5:c.255T>C ENSP00000471030.1:p.Leu85=
ENST00000536250.1:c.*257T>C ENSP00000471120.1:n.*257T>C
ENST00000536670.5:n.281T>C
ENST00000537782.5:c.255T>C ENSP00000469951.1:p.Leu85=
ENST00000538594.5:c.255T>C ENSP00000440939.1:p.Leu85=
ENST00000541135.5:c.255T>C ENSP00000443130.1:p.Leu85=
ENST00000542074.1:c.36+7661T>C ENSP00000469670.1:n.36+7661T>C
ENST00000542794.5:c.*257T>C ENSP00000439983.1:n.*257T>C
ENST00000543044.2:c.219T>C ENSP00000440219.1:p.Leu73=
ENST00000543265.1:c.255T>C ENSP00000443660.1:p.Leu85=
ENST00000544025.5:n.350T>C
ENST00000544801.5:c.255T>C ENSP00000442581.1:p.Leu85=
ENST00000544880.1:n.259T>C
NM_017841.2:c.255T>C , LRG_519t1:c.255T>C NP_060311.1:p.Leu85=
NM_017841.4:c.255T>C MANE Select NP_060311.1:p.Leu85=