Canonical Allele Identifier: CA380683487

Gene: SDHAF2

Linked Data

• MyVariant Identifiers: chr11:g.61205238G>T (hg19) ; chr11:g.61437766G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61437766G>T , CM000673.2:g.61437766G>T	GRCh38
NC_000011.9:g.61205238G>T , CM000673.1:g.61205238G>T	GRCh37
NC_000011.8:g.60961814G>T	NCBI36
NG_023393.1:g.12642G>T , LRG_519:g.12642G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.178G>T MANE Select	ENSP00000301761.3:p.Asp60Tyr
ENST00000301761.6:c.178G>T	ENSP00000301761.2:p.Asp60Tyr
ENST00000359614.9:c.178G>T	ENSP00000352630.5:p.Asp60Tyr
ENST00000534878.5:c.178G>T	ENSP00000471030.1:p.Asp60Tyr
ENST00000536250.1:c.*180G>T	ENSP00000471120.1:n.*180G>T
ENST00000536670.5:n.204G>T
ENST00000537782.5:c.178G>T	ENSP00000469951.1:p.Asp60Tyr
ENST00000538594.5:c.178G>T	ENSP00000440939.1:p.Asp60Tyr
ENST00000541135.5:c.178G>T	ENSP00000443130.1:p.Asp60Tyr
ENST00000542074.1:c.36+7584G>T	ENSP00000469670.1:n.36+7584G>T
ENST00000542794.5:c.*180G>T	ENSP00000439983.1:n.*180G>T
ENST00000543044.2:c.142G>T	ENSP00000440219.1:p.Asp48Tyr
ENST00000543265.1:c.178G>T	ENSP00000443660.1:p.Asp60Tyr
ENST00000544025.5:n.273G>T
ENST00000544801.5:c.178G>T	ENSP00000442581.1:p.Asp60Tyr
ENST00000544880.1:n.182G>T
NM_017841.2:c.178G>T , LRG_519t1:c.178G>T	NP_060311.1:p.Asp60Tyr
NM_017841.4:c.178G>T MANE Select	NP_060311.1:p.Asp60Tyr