Canonical Allele Identifier: CA2000552859
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112093671_112093672delinsTA , CM000673.2:g.112093671_112093672delinsTA GRCh38
NC_000011.9:g.111964395_111964396delinsTA , CM000673.1:g.111964395_111964396delinsTA GRCh37
NC_000011.8:g.111469605_111469606delinsTA NCBI36
NG_012337.2:g.11825_11826delinsTA
NG_012337.3:g.11825_11826delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.*54-1134_*54-1133delinsTA ENSP00000432946.2:n.*54-1134_*54-1133delinsTA
ENST00000534010.2:c.314+4660_314+4661delinsTA ENSP00000433202.2:n.314+4660_314+4661delinsTA
ENST00000375549.8:c.315-1134_315-1133delinsTA MANE Select ENSP00000364699.3:n.315-1134_315-1133delinsTA
ENST00000528021.6:c.314+4660_314+4661delinsTA ENSP00000432465.1:n.314+4660_314+4661delinsTA
ENST00000375549.7:c.315-1134_315-1133delinsTA ENSP00000364699.3:n.315-1134_315-1133delinsTA
ENST00000525291.5:c.198-1134_198-1133delinsTA ENSP00000436669.1:n.198-1134_198-1133delinsTA
ENST00000525987.5:n.319+4660_319+4661delinsTA
ENST00000526592.5:c.*12+462_*12+463delinsTA ENSP00000432005.1:n.*12+462_*12+463delinsTA
ENST00000528021.5:c.314+4660_314+4661delinsTA ENSP00000432465.1:n.314+4660_314+4661delinsTA
ENST00000528048.5:c.170-1134_170-1133delinsTA ENSP00000436217.1:n.170-1134_170-1133delinsTA
ENST00000528182.5:c.308-1134_308-1133delinsTA ENSP00000435475.1:n.308-1134_308-1133delinsTA
ENST00000530923.5:c.359-1134_359-1133delinsTA
ENST00000531744.5:c.314+4660_314+4661delinsTA ENSP00000456957.1:n.314+4660_314+4661delinsTA
ENST00000532699.1:c.314+4660_314+4661delinsTA ENSP00000456434.1:n.314+4660_314+4661delinsTA
ENST00000534010.1:c.145+4660_145+4661delinsTA
NM_001276503.1:c.170-1134_170-1133delinsTA NP_001263432.1:n.170-1134_170-1133delinsTA
NM_001276504.1:c.198-1134_198-1133delinsTA NP_001263433.1:n.198-1134_198-1133delinsTA
NM_001276506.1:c.*12+462_*12+463delinsTA NP_001263435.1:n.*12+462_*12+463delinsTA
NM_003002.3:c.315-1134_315-1133delinsTA NP_002993.1:n.315-1134_315-1133delinsTA
NR_077060.1:n.453-1134_453-1133delinsTA
NM_003002.4:c.315-1134_315-1133delinsTA MANE Select NP_002993.1:n.315-1134_315-1133delinsTA
NM_001276503.2:c.170-1134_170-1133delinsTA NP_001263432.1:n.170-1134_170-1133delinsTA
NM_001276504.2:c.198-1134_198-1133delinsTA NP_001263433.1:n.198-1134_198-1133delinsTA
NM_001276506.2:c.*12+462_*12+463delinsTA NP_001263435.1:n.*12+462_*12+463delinsTA
NR_077060.2:n.404-1134_404-1133delinsTA