Canonical Allele Identifier: CA1202708169

Gene: SDHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161356799T= , CM000663.2:g.161356799T=	GRCh38
NC_000001.10:g.161326589T= , CM000663.1:g.161326589T=	GRCh37
NC_000001.9:g.159593213T=	NCBI36
NG_012767.1:g.47424T= , LRG_317:g.47424T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*365T=	ENSP00000482902.2:n.*365T=
ENST00000367975.7:c.364T= MANE Select	ENSP00000356953.3:p.Phe122=
ENST00000342751.8:c.242-5530T=	ENSP00000356952.3:n.242-5530T=
ENST00000367975.6:c.364T=	ENSP00000356953.2:p.Phe122=
ENST00000392169.6:c.205T=	ENSP00000376009.2:p.Phe69=
ENST00000432287.6:c.262T=	ENSP00000390558.2:p.Phe88=
ENST00000470743.4:c.462T=
ENST00000504963.5:c.*187T=	ENSP00000423929.1:n.*187T=
ENST00000513009.5:c.140-5530T=	ENSP00000423260.1:n.140-5530T=
NM_001035511.1:c.242-5530T=	NP_001030588.1:n.242-5530T=
NM_001035512.1:c.262T=	NP_001030589.1:p.Phe88=
NM_001035513.1:c.205T=	NP_001030590.1:p.Phe69=
NM_001278172.1:c.140-5530T=	NP_001265101.1:n.140-5530T=
NM_003001.3:c.364T= , LRG_317t1:c.364T=	NP_002992.1:p.Phe122=
NR_103459.1:n.421T=
NM_001035511.2:c.242-5530T=	NP_001030588.1:n.242-5530T=
NM_001035512.2:c.262T=	NP_001030589.1:p.Phe88=
NM_001035513.2:c.205T=	NP_001030590.1:p.Phe69=
NM_001278172.2:c.140-5530T=	NP_001265101.1:n.140-5530T=
NM_003001.5:c.364T= MANE Select	NP_002992.1:p.Phe122=
NR_103459.2:n.416T=