Canonical Allele Identifier: CA2695215331
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112094807del , CM000673.2:g.112094807del GRCh38
NC_000011.9:g.111965531del , CM000673.1:g.111965531del GRCh37
NC_000011.8:g.111470741del NCBI36
NG_012337.2:g.12961del
NG_012337.3:g.12961del

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.*56del
ENST00000534010.2:c.314+5796del ENSP00000433202.2:n.314+5796del
ENST00000375549.8:c.317del
ENST00000528021.6:c.314+5796del ENSP00000432465.1:n.314+5796del
ENST00000375549.7:c.317del
ENST00000525291.5:c.200del
ENST00000525987.5:n.319+5796del
ENST00000526592.5:c.*15del
ENST00000528021.5:c.314+5796del ENSP00000432465.1:n.314+5796del
ENST00000528048.5:c.172del
ENST00000528182.5:c.310del
ENST00000530923.5:c.361del
ENST00000531744.5:c.314+5796del ENSP00000456957.1:n.314+5796del
ENST00000532699.1:c.314+5796del ENSP00000456434.1:n.314+5796del
ENST00000534010.1:c.145+5796del
NM_001276503.1:c.172del
NM_001276504.1:c.200del
NM_001276506.1:c.*15del
NM_003002.3:c.317del
NR_077060.1:n.455del
NM_003002.4:c.317del
NM_001276503.2:c.172del
NM_001276504.2:c.200del
NM_001276506.2:c.*15del
NR_077060.2:n.406del