Canonical Allele Identifier: CA1148224789

Gene: SDHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161328466C= , CM000663.2:g.161328466C=	GRCh38
NC_000001.10:g.161298256C= , CM000663.1:g.161298256C=	GRCh37
NC_000001.9:g.159564880C=	NCBI36
NG_012767.1:g.19091C= , LRG_317:g.19091C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*149C=	ENSP00000482902.2:n.*149C=
ENST00000367975.7:c.148C= MANE Select	ENSP00000356953.3:p.Arg50=
ENST00000342751.8:c.148C=	ENSP00000356952.3:p.Arg50=
ENST00000367975.6:c.148C=	ENSP00000356953.2:p.Arg50=
ENST00000392169.6:c.21-12128C=	ENSP00000376009.2:n.21-12128C=
ENST00000432287.6:c.77+4796C=	ENSP00000390558.2:n.77+4796C=
ENST00000470743.4:c.246C=
ENST00000504963.5:c.148C=	ENSP00000423929.1:p.Arg50=
ENST00000513009.5:c.77+4796C=	ENSP00000423260.1:n.77+4796C=
ENST00000515731.1:n.622C=
NM_001035511.1:c.148C=	NP_001030588.1:p.Arg50=
NM_001035512.1:c.77+4796C=	NP_001030589.1:n.77+4796C=
NM_001035513.1:c.21-12128C=	NP_001030590.1:n.21-12128C=
NM_001278172.1:c.77+4796C=	NP_001265101.1:n.77+4796C=
NM_003001.3:c.148C= , LRG_317t1:c.148C=	NP_002992.1:p.Arg50=
NR_103459.1:n.178C=
NM_001035511.2:c.148C=	NP_001030588.1:p.Arg50=
NM_001035512.2:c.77+4796C=	NP_001030589.1:n.77+4796C=
NM_001035513.2:c.21-12128C=	NP_001030590.1:n.21-12128C=
NM_001278172.2:c.77+4796C=	NP_001265101.1:n.77+4796C=
NM_003001.5:c.148C= MANE Select	NP_002992.1:p.Arg50=
NR_103459.2:n.173C=