Canonical Allele Identifier: CA1202708172

Gene: SDHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161356803C= , CM000663.2:g.161356803C=	GRCh38
NC_000001.10:g.161326593C= , CM000663.1:g.161326593C=	GRCh37
NC_000001.9:g.159593217C=	NCBI36
NG_012767.1:g.47428C= , LRG_317:g.47428C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*369C=	ENSP00000482902.2:n.*369C=
ENST00000367975.7:c.368C= MANE Select	ENSP00000356953.3:p.Pro123=
ENST00000342751.8:c.242-5526C=	ENSP00000356952.3:n.242-5526C=
ENST00000367975.6:c.368C=	ENSP00000356953.2:p.Pro123=
ENST00000392169.6:c.209C=	ENSP00000376009.2:p.Pro70=
ENST00000432287.6:c.266C=	ENSP00000390558.2:p.Pro89=
ENST00000470743.4:c.466C=
ENST00000504963.5:c.*191C=	ENSP00000423929.1:n.*191C=
ENST00000513009.5:c.140-5526C=	ENSP00000423260.1:n.140-5526C=
NM_001035511.1:c.242-5526C=	NP_001030588.1:n.242-5526C=
NM_001035512.1:c.266C=	NP_001030589.1:p.Pro89=
NM_001035513.1:c.209C=	NP_001030590.1:p.Pro70=
NM_001278172.1:c.140-5526C=	NP_001265101.1:n.140-5526C=
NM_003001.3:c.368C= , LRG_317t1:c.368C=	NP_002992.1:p.Pro123=
NR_103459.1:n.425C=
NM_001035511.2:c.242-5526C=	NP_001030588.1:n.242-5526C=
NM_001035512.2:c.266C=	NP_001030589.1:p.Pro89=
NM_001035513.2:c.209C=	NP_001030590.1:p.Pro70=
NM_001278172.2:c.140-5526C=	NP_001265101.1:n.140-5526C=
NM_003001.5:c.368C= MANE Select	NP_002992.1:p.Pro123=
NR_103459.2:n.420C=