Canonical Allele Identifier: CA016383
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 189840
ClinVar RCV Id: RCV000170331 RCV000492519
dbSNP Id: rs786205146
MyVariant Identifiers: chr1:g.161284201del (hg19) chr1:g.161314411del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161314411del , CM000663.2:g.161314411del GRCh38
NC_000001.10:g.161284201del , CM000663.1:g.161284201del GRCh37
NC_000001.9:g.159550825del NCBI36
NG_008055.1:g.562del , LRG_256:g.562del
NG_012767.1:g.5036del , LRG_317:g.5036del

Transcript Alleles

HGVS Amino-acid change
ENST00000470743.5:c.6del ENSP00000482902.2:p.Ala3ArgfsTer4
ENST00000367975.7:c.6del MANE Select ENSP00000356953.3:p.Ala3ArgfsTer4
ENST00000342751.8:c.6del ENSP00000356952.3:p.Ala3ArgfsTer4
ENST00000367975.6:c.6del ENSP00000356953.2:p.Ala3ArgfsTer4
ENST00000392169.6:c.6del ENSP00000376009.2:p.Ala3ArgfsTer4
ENST00000432287.6:c.6del ENSP00000390558.2:p.Ala3ArgfsTer4
ENST00000504963.5:c.6del ENSP00000423929.1:p.Ala3ArgfsTer4
ENST00000513009.5:c.6del ENSP00000423260.1:p.Ala3ArgfsTer4
ENST00000515731.1:n.31del
NM_001035511.1:c.6del NP_001030588.1:p.Ala3ArgfsTer4
NM_001035512.1:c.6del NP_001030589.1:p.Ala3ArgfsTer4
NM_001035513.1:c.6del NP_001030590.1:p.Ala3ArgfsTer4
NM_001278172.1:c.6del NP_001265101.1:p.Ala3ArgfsTer4
NM_003001.3:c.6del , LRG_317t1:c.6del NP_002992.1:p.Ala3ArgfsTer4
NR_103459.1:n.36del
NM_001035511.2:c.6del NP_001030588.1:p.Ala3ArgfsTer4
NM_001035512.2:c.6del NP_001030589.1:p.Ala3ArgfsTer4
NM_001035513.2:c.6del NP_001030590.1:p.Ala3ArgfsTer4
NM_001278172.2:c.6del NP_001265101.1:p.Ala3ArgfsTer4
NM_003001.5:c.6del MANE Select NP_002992.1:p.Ala3ArgfsTer4
NR_103459.2:n.31del
Search 100 bp 5'
Search 100 bp 3'