Canonical Allele Identifier: CA10582865
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 239460
ClinVar RCV Id: RCV000232971
dbSNP Id: rs878854589
MyVariant Identifiers: chr11:g.111957641dupC (hg19) chr11:g.112086917dupC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086917dup , CM000673.2:g.112086917dup GRCh38
NC_000011.9:g.111957641dup , CM000673.1:g.111957641dup GRCh37
NC_000011.8:g.111462851dup NCBI36
NG_012337.2:g.5071dup
NG_033145.1:g.4882dup
NG_012337.3:g.5071dup

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.10dup ENSP00000432946.2:p.Leu4ProfsTer?
ENST00000534010.2:c.10dup ENSP00000433202.2:p.Leu4ProfsTer?
ENST00000375549.8:c.10dup MANE Select ENSP00000364699.3:p.Leu4ProfsTer?
ENST00000528021.6:c.10dup ENSP00000432465.1:p.Leu4ProfsTer?
ENST00000640554.1:c.10dup ENSP00000491141.1:p.Leu4ProfsTer?
ENST00000375549.7:c.10dup ENSP00000364699.3:p.Leu4ProfsTer?
ENST00000525291.5:c.10dup ENSP00000436669.1:p.Leu4ProfsTer26
ENST00000525987.5:n.15dup
ENST00000526592.5:c.10dup ENSP00000432005.1:p.Leu4ProfsTer?
ENST00000528021.5:c.10dup ENSP00000432465.1:p.Leu4ProfsTer?
ENST00000528048.5:c.10dup ENSP00000436217.1:p.Leu4ProfsTer?
ENST00000528182.5:c.10dup ENSP00000435475.1:p.Leu4ProfsTer?
ENST00000531744.5:c.10dup ENSP00000456957.1:p.Leu4ProfsTer?
ENST00000532699.1:c.10dup ENSP00000456434.1:p.Leu4ProfsTer?
ENST00000614349.4:c.10dup ENSP00000480666.1:p.Leu4ProfsTer?
NM_001276503.1:c.10dup NP_001263432.1:p.Leu4ProfsTer?
NM_001276504.1:c.10dup NP_001263433.1:p.Leu4ProfsTer26
NM_001276506.1:c.10dup NP_001263435.1:p.Leu4ProfsTer?
NM_003002.3:c.10dup NP_002993.1:p.Leu4ProfsTer?
NR_077060.1:n.94dup
NM_003002.4:c.10dup MANE Select NP_002993.1:p.Leu4ProfsTer?
NM_001276503.2:c.10dup NP_001263432.1:p.Leu4ProfsTer?
NM_001276504.2:c.10dup NP_001263433.1:p.Leu4ProfsTer26
NM_001276506.2:c.10dup NP_001263435.1:p.Leu4ProfsTer?
NR_077060.2:n.45dup
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