Canonical Allele Identifier: CA017100
Gene: SDHD HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 6908
dbSNP Id: rs397514034

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112087898_112087899del , CM000673.2:g.112087898_112087899del GRCh38
NC_000011.9:g.111958622_111958623del , CM000673.1:g.111958622_111958623del GRCh37
NC_000011.8:g.111463832_111463833del NCBI36
NG_012337.2:g.6052_6053del
NG_033145.1:g.3902_3903del
NG_012337.3:g.6052_6053del

Transcript Alleles

HGVS Amino-acid change
NM_001276503.1:c.94_95del VV NP_001263432.1:p.Ala33IlefsTer?
NM_001276504.1:c.52+939_52+940del VV NP_001263433.1:p.=
NM_001276506.1:c.94_95del VV NP_001263435.1:p.Ala33IlefsTer?
NM_003002.3:c.94_95del VV NP_002993.1:p.Ala33IlefsTer?
NR_077060.1:n.178_179del
NM_003002.4:c.94_95del VV MANE Preferred
ENST00000375549.7:c.94_95del ENSP00000364699.3:p.Ala33IlefsTer?
ENST00000525291.5:c.52+939_52+940del ENSP00000436669.1:p.=
ENST00000525987.5:n.99_100del
ENST00000526592.5:c.94_95del ENSP00000432005.1:p.Ala33IlefsTer?
ENST00000528021.5:c.94_95del ENSP00000432465.1:p.Ala33IlefsTer?
ENST00000528048.5:c.94_95del ENSP00000436217.1:p.Ala33IlefsTer?
ENST00000528182.5:c.94_95del ENSP00000435475.1:p.Ala33IlefsTer?
ENST00000530923.5:n.84_85del
ENST00000531744.5:c.94_95del ENSP00000456957.1:p.Ala33IlefsTer?
ENST00000532699.1:c.94_95del ENSP00000456434.1:p.Ala33IlefsTer?
ENST00000614349.4:c.94_95del ENSP00000480666.1:p.Ala33IlefsTer?