Canonical Allele Identifier: CA1202696214

Gene: SDHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161328414C= , CM000663.2:g.161328414C=	GRCh38
NC_000001.10:g.161298204C= , CM000663.1:g.161298204C=	GRCh37
NC_000001.9:g.159564828C=	NCBI36
NG_012767.1:g.19039C= , LRG_317:g.19039C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*97C=	ENSP00000482902.2:n.*97C=
ENST00000367975.7:c.96C= MANE Select	ENSP00000356953.3:p.Thr32=
ENST00000342751.8:c.96C=	ENSP00000356952.3:p.Thr32=
ENST00000367975.6:c.96C=	ENSP00000356953.2:p.Thr32=
ENST00000392169.6:c.21-12180C=	ENSP00000376009.2:n.21-12180C=
ENST00000432287.6:c.77+4744C=	ENSP00000390558.2:n.77+4744C=
ENST00000470743.4:c.194C=
ENST00000504963.5:c.96C=	ENSP00000423929.1:p.Thr32=
ENST00000513009.5:c.77+4744C=	ENSP00000423260.1:n.77+4744C=
ENST00000515731.1:n.570C=
NM_001035511.1:c.96C=	NP_001030588.1:p.Thr32=
NM_001035512.1:c.77+4744C=	NP_001030589.1:n.77+4744C=
NM_001035513.1:c.21-12180C=	NP_001030590.1:n.21-12180C=
NM_001278172.1:c.77+4744C=	NP_001265101.1:n.77+4744C=
NM_003001.3:c.96C= , LRG_317t1:c.96C=	NP_002992.1:p.Thr32=
NR_103459.1:n.126C=
NM_001035511.2:c.96C=	NP_001030588.1:p.Thr32=
NM_001035512.2:c.77+4744C=	NP_001030589.1:n.77+4744C=
NM_001035513.2:c.21-12180C=	NP_001030590.1:n.21-12180C=
NM_001278172.2:c.77+4744C=	NP_001265101.1:n.77+4744C=
NM_003001.5:c.96C= MANE Select	NP_002992.1:p.Thr32=
NR_103459.2:n.121C=