Canonical Allele Identifier: CA2746372099
Gene: SDHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161357071del , CM000663.2:g.161357071del GRCh38
NC_000001.10:g.161326861del , CM000663.1:g.161326861del GRCh37
NC_000001.9:g.159593485del NCBI36
NG_012767.1:g.47696del , LRG_317:g.47696del

Transcript Alleles

HGVS Amino-acid Change
ENST00000470743.5:c.*406+231del ENSP00000482902.2:n.*406+231del
ENST00000367975.7:c.405+231del MANE Select ENSP00000356953.3:n.405+231del
ENST00000342751.8:c.242-5258del ENSP00000356952.3:n.242-5258del
ENST00000367975.6:c.405+231del ENSP00000356953.2:n.405+231del
ENST00000392169.6:c.246+231del ENSP00000376009.2:n.246+231del
ENST00000432287.6:c.303+231del ENSP00000390558.2:n.303+231del
ENST00000470743.4:c.503+231del
ENST00000504963.5:c.*228+231del ENSP00000423929.1:n.*228+231del
ENST00000513009.5:c.140-5258del ENSP00000423260.1:n.140-5258del
NM_001035511.1:c.242-5258del NP_001030588.1:n.242-5258del
NM_001035512.1:c.303+231del NP_001030589.1:n.303+231del
NM_001035513.1:c.246+231del NP_001030590.1:n.246+231del
NM_001278172.1:c.140-5258del NP_001265101.1:n.140-5258del
NM_003001.3:c.405+231del , LRG_317t1:c.405+231del NP_002992.1:n.405+231del
NR_103459.1:n.462+231del
NM_001035511.2:c.242-5258del NP_001030588.1:n.242-5258del
NM_001035512.2:c.303+231del NP_001030589.1:n.303+231del
NM_001035513.2:c.246+231del NP_001030590.1:n.246+231del
NM_001278172.2:c.140-5258del NP_001265101.1:n.140-5258del
NM_003001.5:c.405+231del MANE Select NP_002992.1:n.405+231del
NR_103459.2:n.457+231del