Canonical Allele Identifier: CA2793647918
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112094579_112094582del , CM000673.2:g.112094579_112094582del GRCh38
NC_000011.9:g.111965303_111965306del , CM000673.1:g.111965303_111965306del GRCh37
NC_000011.8:g.111470513_111470516del NCBI36
NG_012337.2:g.12733_12736del
NG_012337.3:g.12733_12736del

Transcript Alleles

HGVS Amino-acid Change
ENST00000530923.6:c.*54-226_*54-223del ENSP00000432946.2:n.*54-226_*54-223del
ENST00000534010.2:c.314+5568_314+5571del ENSP00000433202.2:n.314+5568_314+5571del
ENST00000375549.8:c.315-226_315-223del MANE Select ENSP00000364699.3:n.315-226_315-223del
ENST00000528021.6:c.314+5568_314+5571del ENSP00000432465.1:n.314+5568_314+5571del
ENST00000375549.7:c.315-226_315-223del ENSP00000364699.3:n.315-226_315-223del
ENST00000525291.5:c.198-226_198-223del ENSP00000436669.1:n.198-226_198-223del
ENST00000525987.5:n.319+5568_319+5571del
ENST00000526592.5:c.*13-226_*13-223del ENSP00000432005.1:n.*13-226_*13-223del
ENST00000528021.5:c.314+5568_314+5571del ENSP00000432465.1:n.314+5568_314+5571del
ENST00000528048.5:c.170-226_170-223del ENSP00000436217.1:n.170-226_170-223del
ENST00000528182.5:c.308-226_308-223del ENSP00000435475.1:n.308-226_308-223del
ENST00000530923.5:c.359-226_359-223del
ENST00000531744.5:c.314+5568_314+5571del ENSP00000456957.1:n.314+5568_314+5571del
ENST00000532699.1:c.314+5568_314+5571del ENSP00000456434.1:n.314+5568_314+5571del
ENST00000534010.1:c.145+5568_145+5571del
NM_001276503.1:c.170-226_170-223del NP_001263432.1:n.170-226_170-223del
NM_001276504.1:c.198-226_198-223del NP_001263433.1:n.198-226_198-223del
NM_001276506.1:c.*13-226_*13-223del NP_001263435.1:n.*13-226_*13-223del
NM_003002.3:c.315-226_315-223del NP_002993.1:n.315-226_315-223del
NR_077060.1:n.453-226_453-223del
NM_003002.4:c.315-226_315-223del MANE Select NP_002993.1:n.315-226_315-223del
NM_001276503.2:c.170-226_170-223del NP_001263432.1:n.170-226_170-223del
NM_001276504.2:c.198-226_198-223del NP_001263433.1:n.198-226_198-223del
NM_001276506.2:c.*13-226_*13-223del NP_001263435.1:n.*13-226_*13-223del
NR_077060.2:n.404-226_404-223del