Canonical Allele Identifier: CA421409245

Gene: SDHC

Linked Data

• MyVariant Identifiers: chr1:g.161310420T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161340630T>G , CM000663.2:g.161340630T>G	GRCh38
NC_000001.10:g.161310420T>G , CM000663.1:g.161310420T>G	GRCh37
NC_000001.9:g.159577044T>G	NCBI36
NG_012767.1:g.31255T>G , LRG_317:g.31255T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*217T>G	ENSP00000482902.2:n.*217T>G
ENST00000367975.7:c.216T>G MANE Select	ENSP00000356953.3:p.Arg72=
ENST00000342751.8:c.216T>G	ENSP00000356952.3:p.Arg72=
ENST00000367975.6:c.216T>G	ENSP00000356953.2:p.Arg72=
ENST00000392169.6:c.57T>G	ENSP00000376009.2:p.Arg19=
ENST00000432287.6:c.114T>G	ENSP00000390558.2:p.Arg38=
ENST00000470743.4:c.314T>G
ENST00000504963.5:c.*39T>G	ENSP00000423929.1:n.*39T>G
ENST00000513009.5:c.114T>G	ENSP00000423260.1:p.Arg38=
NM_001035511.1:c.216T>G	NP_001030588.1:p.Arg72=
NM_001035512.1:c.114T>G	NP_001030589.1:p.Arg38=
NM_001035513.1:c.57T>G	NP_001030590.1:p.Arg19=
NM_001278172.1:c.114T>G	NP_001265101.1:p.Arg38=
NM_003001.3:c.216T>G , LRG_317t1:c.216T>G	NP_002992.1:p.Arg72=
NR_103459.1:n.273T>G
NM_001035511.2:c.216T>G	NP_001030588.1:p.Arg72=
NM_001035512.2:c.114T>G	NP_001030589.1:p.Arg38=
NM_001035513.2:c.57T>G	NP_001030590.1:p.Arg19=
NM_001278172.2:c.114T>G	NP_001265101.1:p.Arg38=
NM_003001.5:c.216T>G MANE Select	NP_002992.1:p.Arg72=
NR_103459.2:n.268T>G