Canonical Allele Identifier: CA1202701833

Gene: SDHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161340642T= , CM000663.2:g.161340642T=	GRCh38
NC_000001.10:g.161310432T= , CM000663.1:g.161310432T=	GRCh37
NC_000001.9:g.159577056T=	NCBI36
NG_012767.1:g.31267T= , LRG_317:g.31267T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000470743.5:c.*229T=	ENSP00000482902.2:n.*229T=
ENST00000367975.7:c.228T= MANE Select	ENSP00000356953.3:p.Ile76=
ENST00000342751.8:c.228T=	ENSP00000356952.3:p.Ile76=
ENST00000367975.6:c.228T=	ENSP00000356953.2:p.Ile76=
ENST00000392169.6:c.69T=	ENSP00000376009.2:p.Ile23=
ENST00000432287.6:c.126T=	ENSP00000390558.2:p.Ile42=
ENST00000470743.4:c.326T=
ENST00000504963.5:c.*51T=	ENSP00000423929.1:n.*51T=
ENST00000513009.5:c.126T=	ENSP00000423260.1:p.Ile42=
NM_001035511.1:c.228T=	NP_001030588.1:p.Ile76=
NM_001035512.1:c.126T=	NP_001030589.1:p.Ile42=
NM_001035513.1:c.69T=	NP_001030590.1:p.Ile23=
NM_001278172.1:c.126T=	NP_001265101.1:p.Ile42=
NM_003001.3:c.228T= , LRG_317t1:c.228T=	NP_002992.1:p.Ile76=
NR_103459.1:n.285T=
NM_001035511.2:c.228T=	NP_001030588.1:p.Ile76=
NM_001035512.2:c.126T=	NP_001030589.1:p.Ile42=
NM_001035513.2:c.69T=	NP_001030590.1:p.Ile23=
NM_001278172.2:c.126T=	NP_001265101.1:p.Ile42=
NM_003001.5:c.228T= MANE Select	NP_002992.1:p.Ile76=
NR_103459.2:n.280T=