Canonical Allele Identifier: CA1144229023

Gene: SDHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161356833G= , CM000663.2:g.161356833G=	GRCh38
NC_000001.10:g.161326623G= , CM000663.1:g.161326623G=	GRCh37
NC_000001.9:g.159593247G=	NCBI36
NG_012767.1:g.47458G= , LRG_317:g.47458G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*399G=	ENSP00000482902.2:n.*399G=
ENST00000367975.7:c.398G= MANE Select	ENSP00000356953.3:p.Arg133=
ENST00000342751.8:c.242-5496G=	ENSP00000356952.3:n.242-5496G=
ENST00000367975.6:c.398G=	ENSP00000356953.2:p.Arg133=
ENST00000392169.6:c.239G=	ENSP00000376009.2:p.Arg80=
ENST00000432287.6:c.296G=	ENSP00000390558.2:p.Arg99=
ENST00000470743.4:c.496G=
ENST00000504963.5:c.*221G=	ENSP00000423929.1:n.*221G=
ENST00000513009.5:c.140-5496G=	ENSP00000423260.1:n.140-5496G=
NM_001035511.1:c.242-5496G=	NP_001030588.1:n.242-5496G=
NM_001035512.1:c.296G=	NP_001030589.1:p.Arg99=
NM_001035513.1:c.239G=	NP_001030590.1:p.Arg80=
NM_001278172.1:c.140-5496G=	NP_001265101.1:n.140-5496G=
NM_003001.3:c.398G= , LRG_317t1:c.398G=	NP_002992.1:p.Arg133=
NR_103459.1:n.455G=
NM_001035511.2:c.242-5496G=	NP_001030588.1:n.242-5496G=
NM_001035512.2:c.296G=	NP_001030589.1:p.Arg99=
NM_001035513.2:c.239G=	NP_001030590.1:p.Arg80=
NM_001278172.2:c.140-5496G=	NP_001265101.1:n.140-5496G=
NM_003001.5:c.398G= MANE Select	NP_002992.1:p.Arg133=
NR_103459.2:n.450G=