Canonical Allele Identifier: CA2000553862
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112094838_112094839delinsTG , CM000673.2:g.112094838_112094839delinsTG GRCh38
NC_000011.9:g.111965562_111965563delinsTG , CM000673.1:g.111965562_111965563delinsTG GRCh37
NC_000011.8:g.111470772_111470773delinsTG NCBI36
NG_012337.2:g.12992_12993delinsTG
NG_012337.3:g.12992_12993delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.*87_*88delinsTG ENSP00000432946.2:n.*87_*88delinsTG
ENST00000534010.2:c.314+5827_314+5828delinsTG ENSP00000433202.2:n.314+5827_314+5828deli...
ENST00000375549.8:c.348_349delinsTG MANE Select ENSP00000364699.3:p.His116=
ENST00000528021.6:c.314+5827_314+5828delinsTG ENSP00000432465.1:n.314+5827_314+5828deli...
ENST00000375549.7:c.348_349delinsTG ENSP00000364699.3:p.His116=
ENST00000525291.5:c.231_232delinsTG ENSP00000436669.1:p.His77=
ENST00000525987.5:n.319+5827_319+5828delinsTG
ENST00000526592.5:c.*46_*47delinsTG ENSP00000432005.1:n.*46_*47delinsTG
ENST00000528021.5:c.314+5827_314+5828delinsTG ENSP00000432465.1:n.314+5827_314+5828deli...
ENST00000528048.5:c.203_204delinsTG ENSP00000436217.1:p.Met68=
ENST00000528182.5:c.341_342delinsTG ENSP00000435475.1:p.Met114=
ENST00000530923.5:c.392_393delinsTG
ENST00000531744.5:c.314+5827_314+5828delinsTG ENSP00000456957.1:n.314+5827_314+5828deli...
ENST00000532699.1:c.314+5827_314+5828delinsTG ENSP00000456434.1:n.314+5827_314+5828deli...
ENST00000534010.1:c.145+5827_145+5828delinsTG
NM_001276503.1:c.203_204delinsTG NP_001263432.1:p.Met68=
NM_001276504.1:c.231_232delinsTG NP_001263433.1:p.His77=
NM_001276506.1:c.*46_*47delinsTG NP_001263435.1:n.*46_*47delinsTG
NM_003002.3:c.348_349delinsTG NP_002993.1:p.His116=
NR_077060.1:n.486_487delinsTG
NM_003002.4:c.348_349delinsTG MANE Select NP_002993.1:p.His116=
NM_001276503.2:c.203_204delinsTG NP_001263432.1:p.Met68=
NM_001276504.2:c.231_232delinsTG NP_001263433.1:p.His77=
NM_001276506.2:c.*46_*47delinsTG NP_001263435.1:n.*46_*47delinsTG
NR_077060.2:n.437_438delinsTG