Canonical Allele Identifier: CA1202708183
Gene: SDHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161356819C= , CM000663.2:g.161356819C= GRCh38
NC_000001.10:g.161326609C= , CM000663.1:g.161326609C= GRCh37
NC_000001.9:g.159593233C= NCBI36
NG_012767.1:g.47444C= , LRG_317:g.47444C=

Transcript Alleles

HGVS Amino-acid change
ENST00000470743.5:c.*385C= ENSP00000482902.2:n.*385C=
ENST00000367975.7:c.384C= MANE Select ENSP00000356953.3:p.Thr128=
ENST00000342751.8:c.242-5510C= ENSP00000356952.3:n.242-5510C=
ENST00000367975.6:c.384C= ENSP00000356953.2:p.Thr128=
ENST00000392169.6:c.225C= ENSP00000376009.2:p.Thr75=
ENST00000432287.6:c.282C= ENSP00000390558.2:p.Thr94=
ENST00000470743.4:c.482C=
ENST00000504963.5:c.*207C= ENSP00000423929.1:n.*207C=
ENST00000513009.5:c.140-5510C= ENSP00000423260.1:n.140-5510C=
NM_001035511.1:c.242-5510C= NP_001030588.1:n.242-5510C=
NM_001035512.1:c.282C= NP_001030589.1:p.Thr94=
NM_001035513.1:c.225C= NP_001030590.1:p.Thr75=
NM_001278172.1:c.140-5510C= NP_001265101.1:n.140-5510C=
NM_003001.3:c.384C= , LRG_317t1:c.384C= NP_002992.1:p.Thr128=
NR_103459.1:n.441C=
NM_001035511.2:c.242-5510C= NP_001030588.1:n.242-5510C=
NM_001035512.2:c.282C= NP_001030589.1:p.Thr94=
NM_001035513.2:c.225C= NP_001030590.1:p.Thr75=
NM_001278172.2:c.140-5510C= NP_001265101.1:n.140-5510C=
NM_003001.5:c.384C= MANE Select NP_002992.1:p.Thr128=
NR_103459.2:n.436C=