Canonical Allele Identifier: CA474802918

Gene: SDHAF2

Linked Data

• MyVariant Identifiers: chr11:g.61205249A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61437777A>C , CM000673.2:g.61437777A>C	GRCh38
NC_000011.9:g.61205249A>C , CM000673.1:g.61205249A>C	GRCh37
NC_000011.8:g.60961825A>C	NCBI36
NG_023393.1:g.12653A>C , LRG_519:g.12653A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.189A>C MANE Select	ENSP00000301761.3:p.Ile63=
ENST00000301761.6:c.189A>C	ENSP00000301761.2:p.Ile63=
ENST00000359614.9:c.189A>C	ENSP00000352630.5:p.Ile63=
ENST00000534878.5:c.189A>C	ENSP00000471030.1:p.Ile63=
ENST00000536250.1:c.*191A>C	ENSP00000471120.1:n.*191A>C
ENST00000536670.5:n.215A>C
ENST00000537782.5:c.189A>C	ENSP00000469951.1:p.Ile63=
ENST00000538594.5:c.189A>C	ENSP00000440939.1:p.Ile63=
ENST00000541135.5:c.189A>C	ENSP00000443130.1:p.Ile63=
ENST00000542074.1:c.36+7595A>C	ENSP00000469670.1:n.36+7595A>C
ENST00000542794.5:c.*191A>C	ENSP00000439983.1:n.*191A>C
ENST00000543044.2:c.153A>C	ENSP00000440219.1:p.Ile51=
ENST00000543265.1:c.189A>C	ENSP00000443660.1:p.Ile63=
ENST00000544025.5:n.284A>C
ENST00000544801.5:c.189A>C	ENSP00000442581.1:p.Ile63=
ENST00000544880.1:n.193A>C
NM_017841.2:c.189A>C , LRG_519t1:c.189A>C	NP_060311.1:p.Ile63=
NM_017841.4:c.189A>C MANE Select	NP_060311.1:p.Ile63=