Canonical Allele Identifier: CA1139655529

Gene: SDHC

Linked Data

• ClinVar Variation Id: 959675
• ClinVar RCV Id: RCV001233063
• dbSNP Id: rs1671157149

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161328493del , CM000663.2:g.161328493del	GRCh38
NC_000001.10:g.161298283del , CM000663.1:g.161298283del	GRCh37
NC_000001.9:g.159564907del	NCBI36
NG_012767.1:g.19118del , LRG_317:g.19118del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*176del	ENSP00000482902.2:n.*176del
ENST00000367975.7:c.175del MANE Select	ENSP00000356953.3:p.Tyr59ThrfsTer20
ENST00000342751.8:c.175del	ENSP00000356952.3:p.Tyr59ThrfsTer20
ENST00000367975.6:c.175del	ENSP00000356953.2:p.Tyr59ThrfsTer20
ENST00000392169.6:c.21-12101del	ENSP00000376009.2:n.21-12101del
ENST00000432287.6:c.77+4823del	ENSP00000390558.2:n.77+4823del
ENST00000470743.4:c.273del
ENST00000504963.5:c.175del	ENSP00000423929.1:p.Tyr59ThrfsTer29
ENST00000513009.5:c.77+4823del	ENSP00000423260.1:n.77+4823del
ENST00000515731.1:n.649del
NM_001035511.1:c.175del	NP_001030588.1:p.Tyr59ThrfsTer20
NM_001035512.1:c.77+4823del	NP_001030589.1:n.77+4823del
NM_001035513.1:c.21-12101del	NP_001030590.1:n.21-12101del
NM_001278172.1:c.77+4823del	NP_001265101.1:n.77+4823del
NM_003001.3:c.175del , LRG_317t1:c.175del	NP_002992.1:p.Tyr59ThrfsTer20
NR_103459.1:n.205del
NM_001035511.2:c.175del	NP_001030588.1:p.Tyr59ThrfsTer20
NM_001035512.2:c.77+4823del	NP_001030589.1:n.77+4823del
NM_001035513.2:c.21-12101del	NP_001030590.1:n.21-12101del
NM_001278172.2:c.77+4823del	NP_001265101.1:n.77+4823del
NM_003001.5:c.175del MANE Select	NP_002992.1:p.Tyr59ThrfsTer20
NR_103459.2:n.200del