Canonical Allele Identifier: CA1202696079
Gene: SDHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161328322_161328325delinsTTAA , CM000663.2:g.161328322_161328325delinsTTAA GRCh38
NC_000001.10:g.161298112_161298115delinsTTAA , CM000663.1:g.161298112_161298115delinsTTAA GRCh37
NC_000001.9:g.159564736_159564739delinsTTAA NCBI36
NG_012767.1:g.18947_18950delinsTTAA , LRG_317:g.18947_18950delinsTTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000470743.5:c.*79-74_*79-71delinsTTAA ENSP00000482902.2:n.*79-74_*79-71delinsTTAA
ENST00000367975.7:c.78-74_78-71delinsTTAA MANE Select ENSP00000356953.3:n.78-74_78-71delinsTTAA
ENST00000342751.8:c.78-74_78-71delinsTTAA ENSP00000356952.3:n.78-74_78-71delinsTTAA
ENST00000367975.6:c.78-74_78-71delinsTTAA ENSP00000356953.2:n.78-74_78-71delinsTTAA
ENST00000392169.6:c.21-12272_21-12269delinsTTAA ENSP00000376009.2:n.21-12272_21-12269delinsTTAA
ENST00000432287.6:c.77+4652_77+4655delinsTTAA ENSP00000390558.2:n.77+4652_77+4655delinsTTAA
ENST00000470743.4:c.176-74_176-71delinsTTAA
ENST00000504963.5:c.78-74_78-71delinsTTAA ENSP00000423929.1:n.78-74_78-71delinsTTAA
ENST00000513009.5:c.77+4652_77+4655delinsTTAA ENSP00000423260.1:n.77+4652_77+4655delinsTTAA
ENST00000515731.1:n.552-74_552-71delinsTTAA
NM_001035511.1:c.78-74_78-71delinsTTAA NP_001030588.1:n.78-74_78-71delinsTTAA
NM_001035512.1:c.77+4652_77+4655delinsTTAA NP_001030589.1:n.77+4652_77+4655delinsTTAA
NM_001035513.1:c.21-12272_21-12269delinsTTAA NP_001030590.1:n.21-12272_21-12269delinsTTAA
NM_001278172.1:c.77+4652_77+4655delinsTTAA NP_001265101.1:n.77+4652_77+4655delinsTTAA
NM_003001.3:c.78-74_78-71delinsTTAA , LRG_317t1:c.78-74_78-71delinsTTAA NP_002992.1:n.78-74_78-71delinsTTAA
NR_103459.1:n.108-74_108-71delinsTTAA
NM_001035511.2:c.78-74_78-71delinsTTAA NP_001030588.1:n.78-74_78-71delinsTTAA
NM_001035512.2:c.77+4652_77+4655delinsTTAA NP_001030589.1:n.77+4652_77+4655delinsTTAA
NM_001035513.2:c.21-12272_21-12269delinsTTAA NP_001030590.1:n.21-12272_21-12269delinsTTAA
NM_001278172.2:c.77+4652_77+4655delinsTTAA NP_001265101.1:n.77+4652_77+4655delinsTTAA
NM_003001.5:c.78-74_78-71delinsTTAA MANE Select NP_002992.1:n.78-74_78-71delinsTTAA
NR_103459.2:n.103-74_103-71delinsTTAA