Canonical Allele Identifier: CA1202701823

Gene: SDHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161340628C= , CM000663.2:g.161340628C=	GRCh38
NC_000001.10:g.161310418C= , CM000663.1:g.161310418C=	GRCh37
NC_000001.9:g.159577042C=	NCBI36
NG_012767.1:g.31253C= , LRG_317:g.31253C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*215C=	ENSP00000482902.2:n.*215C=
ENST00000367975.7:c.214C= MANE Select	ENSP00000356953.3:p.Arg72=
ENST00000342751.8:c.214C=	ENSP00000356952.3:p.Arg72=
ENST00000367975.6:c.214C=	ENSP00000356953.2:p.Arg72=
ENST00000392169.6:c.55C=	ENSP00000376009.2:p.Arg19=
ENST00000432287.6:c.112C=	ENSP00000390558.2:p.Arg38=
ENST00000470743.4:c.312C=
ENST00000504963.5:c.*37C=	ENSP00000423929.1:n.*37C=
ENST00000513009.5:c.112C=	ENSP00000423260.1:p.Arg38=
NM_001035511.1:c.214C=	NP_001030588.1:p.Arg72=
NM_001035512.1:c.112C=	NP_001030589.1:p.Arg38=
NM_001035513.1:c.55C=	NP_001030590.1:p.Arg19=
NM_001278172.1:c.112C=	NP_001265101.1:p.Arg38=
NM_003001.3:c.214C= , LRG_317t1:c.214C=	NP_002992.1:p.Arg72=
NR_103459.1:n.271C=
NM_001035511.2:c.214C=	NP_001030588.1:p.Arg72=
NM_001035512.2:c.112C=	NP_001030589.1:p.Arg38=
NM_001035513.2:c.55C=	NP_001030590.1:p.Arg19=
NM_001278172.2:c.112C=	NP_001265101.1:p.Arg38=
NM_003001.5:c.214C= MANE Select	NP_002992.1:p.Arg72=
NR_103459.2:n.266C=