Canonical Allele Identifier: CA1202696453
Gene: SDHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161328521_161328525delinsAGAAT , CM000663.2:g.161328521_161328525delinsAGAAT GRCh38
NC_000001.10:g.161298311_161298315delinsAGAAT , CM000663.1:g.161298311_161298315delinsAGAAT GRCh37
NC_000001.9:g.159564935_159564939delinsAGAAT NCBI36
NG_012767.1:g.19146_19150delinsAGAAT , LRG_317:g.19146_19150delinsAGAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000470743.5:c.*180+24_*180+28delinsAGAAT ENSP00000482902.2:n.*180+24_*180+28delinsAGAAT
ENST00000367975.7:c.179+24_179+28delinsAGAAT MANE Select ENSP00000356953.3:n.179+24_179+28delinsAGAAT
ENST00000342751.8:c.179+24_179+28delinsAGAAT ENSP00000356952.3:n.179+24_179+28delinsAGAAT
ENST00000367975.6:c.179+24_179+28delinsAGAAT ENSP00000356953.2:n.179+24_179+28delinsAGAAT
ENST00000392169.6:c.21-12073_21-12069delinsAGAAT ENSP00000376009.2:n.21-12073_21-12069delinsAGAAT
ENST00000432287.6:c.77+4851_77+4855delinsAGAAT ENSP00000390558.2:n.77+4851_77+4855delinsAGAAT
ENST00000470743.4:c.277+24_277+28delinsAGAAT
ENST00000504963.5:c.179+24_179+28delinsAGAAT ENSP00000423929.1:n.179+24_179+28delinsAGAAT
ENST00000513009.5:c.77+4851_77+4855delinsAGAAT ENSP00000423260.1:n.77+4851_77+4855delinsAGAAT
NM_001035511.1:c.179+24_179+28delinsAGAAT NP_001030588.1:n.179+24_179+28delinsAGAAT
NM_001035512.1:c.77+4851_77+4855delinsAGAAT NP_001030589.1:n.77+4851_77+4855delinsAGAAT
NM_001035513.1:c.21-12073_21-12069delinsAGAAT NP_001030590.1:n.21-12073_21-12069delinsAGAAT
NM_001278172.1:c.77+4851_77+4855delinsAGAAT NP_001265101.1:n.77+4851_77+4855delinsAGAAT
NM_003001.3:c.179+24_179+28delinsAGAAT , LRG_317t1:c.179+24_179+28delinsAGAAT NP_002992.1:n.179+24_179+28delinsAGAAT
NR_103459.1:n.209+24_209+28delinsAGAAT
NM_001035511.2:c.179+24_179+28delinsAGAAT NP_001030588.1:n.179+24_179+28delinsAGAAT
NM_001035512.2:c.77+4851_77+4855delinsAGAAT NP_001030589.1:n.77+4851_77+4855delinsAGAAT
NM_001035513.2:c.21-12073_21-12069delinsAGAAT NP_001030590.1:n.21-12073_21-12069delinsAGAAT
NM_001278172.2:c.77+4851_77+4855delinsAGAAT NP_001265101.1:n.77+4851_77+4855delinsAGAAT
NM_003001.5:c.179+24_179+28delinsAGAAT MANE Select NP_002992.1:n.179+24_179+28delinsAGAAT
NR_103459.2:n.204+24_204+28delinsAGAAT