Canonical Allele Identifier: CA2544253888
Gene: SDHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161357089_161357090insGCCCAG , CM000663.2:g.161357089_161357090insGCCCAG GRCh38
NC_000001.10:g.161326879_161326880insGCCCAG , CM000663.1:g.161326879_161326880insGCCCAG GRCh37
NC_000001.9:g.159593503_159593504insGCCCAG NCBI36
NG_012767.1:g.47714_47715insGCCCAG , LRG_317:g.47714_47715insGCCCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000470743.5:c.*406+249_*406+250insGCCCAG ENSP00000482902.2:n.*406+249_*406+250insGCCCAG
ENST00000367975.7:c.405+249_405+250insGCCCAG MANE Select ENSP00000356953.3:n.405+249_405+250insGCCCAG
ENST00000342751.8:c.242-5240_242-5239insGCCCAG ENSP00000356952.3:n.242-5240_242-5239insGCCCAG
ENST00000367975.6:c.405+249_405+250insGCCCAG ENSP00000356953.2:n.405+249_405+250insGCCCAG
ENST00000392169.6:c.246+249_246+250insGCCCAG ENSP00000376009.2:n.246+249_246+250insGCCCAG
ENST00000432287.6:c.303+249_303+250insGCCCAG ENSP00000390558.2:n.303+249_303+250insGCCCAG
ENST00000470743.4:c.503+249_503+250insGCCCAG
ENST00000504963.5:c.*228+249_*228+250insGCCCAG ENSP00000423929.1:n.*228+249_*228+250insGCCCAG
ENST00000513009.5:c.140-5240_140-5239insGCCCAG ENSP00000423260.1:n.140-5240_140-5239insGCCCAG
NM_001035511.1:c.242-5240_242-5239insGCCCAG NP_001030588.1:n.242-5240_242-5239insGCCCAG
NM_001035512.1:c.303+249_303+250insGCCCAG NP_001030589.1:n.303+249_303+250insGCCCAG
NM_001035513.1:c.246+249_246+250insGCCCAG NP_001030590.1:n.246+249_246+250insGCCCAG
NM_001278172.1:c.140-5240_140-5239insGCCCAG NP_001265101.1:n.140-5240_140-5239insGCCCAG
NM_003001.3:c.405+249_405+250insGCCCAG , LRG_317t1:c.405+249_405+250insGCCCAG NP_002992.1:n.405+249_405+250insGCCCAG
NR_103459.1:n.462+249_462+250insGCCCAG
NM_001035511.2:c.242-5240_242-5239insGCCCAG NP_001030588.1:n.242-5240_242-5239insGCCCAG
NM_001035512.2:c.303+249_303+250insGCCCAG NP_001030589.1:n.303+249_303+250insGCCCAG
NM_001035513.2:c.246+249_246+250insGCCCAG NP_001030590.1:n.246+249_246+250insGCCCAG
NM_001278172.2:c.140-5240_140-5239insGCCCAG NP_001265101.1:n.140-5240_140-5239insGCCCAG
NM_003001.5:c.405+249_405+250insGCCCAG MANE Select NP_002992.1:n.405+249_405+250insGCCCAG
NR_103459.2:n.457+249_457+250insGCCCAG