Canonical Allele Identifier: CA2000553781
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112094817_112094820delinsAGTT , CM000673.2:g.112094817_112094820delinsAGTT GRCh38
NC_000011.9:g.111965541_111965544delinsAGTT , CM000673.1:g.111965541_111965544delinsAGTT GRCh37
NC_000011.8:g.111470751_111470754delinsAGTT NCBI36
NG_012337.2:g.12971_12974delinsAGTT
NG_012337.3:g.12971_12974delinsAGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000530923.6:c.*66_*69delinsAGTT ENSP00000432946.2:n.*66_*69delinsAGTT
ENST00000534010.2:c.314+5806_314+5809delinsAGTT ENSP00000433202.2:n.314+5806_314+5809delinsAGTT
ENST00000375549.8:c.327_330delinsAGTT MANE Select ENSP00000364699.3:p.Gln109=
ENST00000528021.6:c.314+5806_314+5809delinsAGTT ENSP00000432465.1:n.314+5806_314+5809delinsAGTT
ENST00000375549.7:c.327_330delinsAGTT ENSP00000364699.3:p.Gln109=
ENST00000525291.5:c.210_213delinsAGTT ENSP00000436669.1:p.Gln70=
ENST00000525987.5:n.319+5806_319+5809delinsAGTT
ENST00000526592.5:c.*25_*28delinsAGTT ENSP00000432005.1:n.*25_*28delinsAGTT
ENST00000528021.5:c.314+5806_314+5809delinsAGTT ENSP00000432465.1:n.314+5806_314+5809delinsAGTT
ENST00000528048.5:c.182_185delinsAGTT ENSP00000436217.1:p.Lys61=
ENST00000528182.5:c.320_323delinsAGTT ENSP00000435475.1:p.Lys107=
ENST00000530923.5:c.371_374delinsAGTT
ENST00000531744.5:c.314+5806_314+5809delinsAGTT ENSP00000456957.1:n.314+5806_314+5809delinsAGTT
ENST00000532699.1:c.314+5806_314+5809delinsAGTT ENSP00000456434.1:n.314+5806_314+5809delinsAGTT
ENST00000534010.1:c.145+5806_145+5809delinsAGTT
NM_001276503.1:c.182_185delinsAGTT NP_001263432.1:p.Lys61=
NM_001276504.1:c.210_213delinsAGTT NP_001263433.1:p.Gln70=
NM_001276506.1:c.*25_*28delinsAGTT NP_001263435.1:n.*25_*28delinsAGTT
NM_003002.3:c.327_330delinsAGTT NP_002993.1:p.Gln109=
NR_077060.1:n.465_468delinsAGTT
NM_003002.4:c.327_330delinsAGTT MANE Select NP_002993.1:p.Gln109=
NM_001276503.2:c.182_185delinsAGTT NP_001263432.1:p.Lys61=
NM_001276504.2:c.210_213delinsAGTT NP_001263433.1:p.Gln70=
NM_001276506.2:c.*25_*28delinsAGTT NP_001263435.1:n.*25_*28delinsAGTT
NR_077060.2:n.416_419delinsAGTT