Canonical Allele Identifier: CA1202708180
Gene: SDHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161356814C= , CM000663.2:g.161356814C= GRCh38
NC_000001.10:g.161326604C= , CM000663.1:g.161326604C= GRCh37
NC_000001.9:g.159593228C= NCBI36
NG_012767.1:g.47439C= , LRG_317:g.47439C=

Transcript Alleles

HGVS Amino-acid change
ENST00000470743.5:c.*380C= ENSP00000482902.2:n.*380C=
ENST00000367975.7:c.379C= MANE Select ENSP00000356953.3:p.His127=
ENST00000342751.8:c.242-5515C= ENSP00000356952.3:n.242-5515C=
ENST00000367975.6:c.379C= ENSP00000356953.2:p.His127=
ENST00000392169.6:c.220C= ENSP00000376009.2:p.His74=
ENST00000432287.6:c.277C= ENSP00000390558.2:p.His93=
ENST00000470743.4:c.477C=
ENST00000504963.5:c.*202C= ENSP00000423929.1:n.*202C=
ENST00000513009.5:c.140-5515C= ENSP00000423260.1:n.140-5515C=
NM_001035511.1:c.242-5515C= NP_001030588.1:n.242-5515C=
NM_001035512.1:c.277C= NP_001030589.1:p.His93=
NM_001035513.1:c.220C= NP_001030590.1:p.His74=
NM_001278172.1:c.140-5515C= NP_001265101.1:n.140-5515C=
NM_003001.3:c.379C= , LRG_317t1:c.379C= NP_002992.1:p.His127=
NR_103459.1:n.436C=
NM_001035511.2:c.242-5515C= NP_001030588.1:n.242-5515C=
NM_001035512.2:c.277C= NP_001030589.1:p.His93=
NM_001035513.2:c.220C= NP_001030590.1:p.His74=
NM_001278172.2:c.140-5515C= NP_001265101.1:n.140-5515C=
NM_003001.5:c.379C= MANE Select NP_002992.1:p.His127=
NR_103459.2:n.431C=