Canonical Allele Identifier: CA1202708181
Gene: SDHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161356815A= , CM000663.2:g.161356815A= GRCh38
NC_000001.10:g.161326605A= , CM000663.1:g.161326605A= GRCh37
NC_000001.9:g.159593229A= NCBI36
NG_012767.1:g.47440A= , LRG_317:g.47440A=

Transcript Alleles

HGVS Amino-acid change
ENST00000470743.5:c.*381A= ENSP00000482902.2:n.*381A=
ENST00000367975.7:c.380A= MANE Select ENSP00000356953.3:p.His127=
ENST00000342751.8:c.242-5514A= ENSP00000356952.3:n.242-5514A=
ENST00000367975.6:c.380A= ENSP00000356953.2:p.His127=
ENST00000392169.6:c.221A= ENSP00000376009.2:p.His74=
ENST00000432287.6:c.278A= ENSP00000390558.2:p.His93=
ENST00000470743.4:c.478A=
ENST00000504963.5:c.*203A= ENSP00000423929.1:n.*203A=
ENST00000513009.5:c.140-5514A= ENSP00000423260.1:n.140-5514A=
NM_001035511.1:c.242-5514A= NP_001030588.1:n.242-5514A=
NM_001035512.1:c.278A= NP_001030589.1:p.His93=
NM_001035513.1:c.221A= NP_001030590.1:p.His74=
NM_001278172.1:c.140-5514A= NP_001265101.1:n.140-5514A=
NM_003001.3:c.380A= , LRG_317t1:c.380A= NP_002992.1:p.His127=
NR_103459.1:n.437A=
NM_001035511.2:c.242-5514A= NP_001030588.1:n.242-5514A=
NM_001035512.2:c.278A= NP_001030589.1:p.His93=
NM_001035513.2:c.221A= NP_001030590.1:p.His74=
NM_001278172.2:c.140-5514A= NP_001265101.1:n.140-5514A=
NM_003001.5:c.380A= MANE Select NP_002992.1:p.His127=
NR_103459.2:n.432A=