Canonical Allele Identifier: CA2838032882
Gene: SDHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161328436dup , CM000663.2:g.161328436dup GRCh38
NC_000001.10:g.161298226dup , CM000663.1:g.161298226dup GRCh37
NC_000001.9:g.159564850dup NCBI36
NG_012767.1:g.19061dup , LRG_317:g.19061dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000470743.5:c.*119dup ENSP00000482902.2:n.*119dup
ENST00000367975.7:c.118dup MANE Select ENSP00000356953.3:p.Arg40ProfsTer5
ENST00000342751.8:c.118dup ENSP00000356952.3:p.Arg40ProfsTer5
ENST00000367975.6:c.118dup ENSP00000356953.2:p.Arg40ProfsTer5
ENST00000392169.6:c.21-12158dup ENSP00000376009.2:n.21-12158dup
ENST00000432287.6:c.77+4766dup ENSP00000390558.2:n.77+4766dup
ENST00000470743.4:c.216dup
ENST00000504963.5:c.118dup ENSP00000423929.1:p.Arg40ProfsTer5
ENST00000513009.5:c.77+4766dup ENSP00000423260.1:n.77+4766dup
ENST00000515731.1:n.592dup
NM_001035511.1:c.118dup NP_001030588.1:p.Arg40ProfsTer5
NM_001035512.1:c.77+4766dup NP_001030589.1:n.77+4766dup
NM_001035513.1:c.21-12158dup NP_001030590.1:n.21-12158dup
NM_001278172.1:c.77+4766dup NP_001265101.1:n.77+4766dup
NM_003001.3:c.118dup , LRG_317t1:c.118dup NP_002992.1:p.Arg40ProfsTer5
NR_103459.1:n.148dup
NM_001035511.2:c.118dup NP_001030588.1:p.Arg40ProfsTer5
NM_001035512.2:c.77+4766dup NP_001030589.1:n.77+4766dup
NM_001035513.2:c.21-12158dup NP_001030590.1:n.21-12158dup
NM_001278172.2:c.77+4766dup NP_001265101.1:n.77+4766dup
NM_003001.5:c.118dup MANE Select NP_002992.1:p.Arg40ProfsTer5
NR_103459.2:n.143dup