Canonical Allele Identifier: CA2000553700
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112094798_112094800delinsTCT , CM000673.2:g.112094798_112094800delinsTCT GRCh38
NC_000011.9:g.111965522_111965524delinsTCT , CM000673.1:g.111965522_111965524delinsTCT GRCh37
NC_000011.8:g.111470732_111470734delinsTCT NCBI36
NG_012337.2:g.12952_12954delinsTCT
NG_012337.3:g.12952_12954delinsTCT

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.*54-7_*54-5delinsTCT ENSP00000432946.2:n.*54-7_*54-5delinsTCT
ENST00000534010.2:c.314+5787_314+5789delinsTCT ENSP00000433202.2:n.314+5787_314+5789deli...
ENST00000375549.8:c.315-7_315-5delinsTCT MANE Select ENSP00000364699.3:n.315-7_315-5delinsTCT
ENST00000528021.6:c.314+5787_314+5789delinsTCT ENSP00000432465.1:n.314+5787_314+5789deli...
ENST00000375549.7:c.315-7_315-5delinsTCT ENSP00000364699.3:n.315-7_315-5delinsTCT
ENST00000525291.5:c.198-7_198-5delinsTCT ENSP00000436669.1:n.198-7_198-5delinsTCT
ENST00000525987.5:n.319+5787_319+5789delinsTCT
ENST00000526592.5:c.*13-7_*13-5delinsTCT ENSP00000432005.1:n.*13-7_*13-5delinsTCT
ENST00000528021.5:c.314+5787_314+5789delinsTCT ENSP00000432465.1:n.314+5787_314+5789deli...
ENST00000528048.5:c.170-7_170-5delinsTCT ENSP00000436217.1:n.170-7_170-5delinsTCT
ENST00000528182.5:c.308-7_308-5delinsTCT ENSP00000435475.1:n.308-7_308-5delinsTCT
ENST00000530923.5:c.359-7_359-5delinsTCT
ENST00000531744.5:c.314+5787_314+5789delinsTCT ENSP00000456957.1:n.314+5787_314+5789deli...
ENST00000532699.1:c.314+5787_314+5789delinsTCT ENSP00000456434.1:n.314+5787_314+5789deli...
ENST00000534010.1:c.145+5787_145+5789delinsTCT
NM_001276503.1:c.170-7_170-5delinsTCT NP_001263432.1:n.170-7_170-5delinsTCT
NM_001276504.1:c.198-7_198-5delinsTCT NP_001263433.1:n.198-7_198-5delinsTCT
NM_001276506.1:c.*13-7_*13-5delinsTCT NP_001263435.1:n.*13-7_*13-5delinsTCT
NM_003002.3:c.315-7_315-5delinsTCT NP_002993.1:n.315-7_315-5delinsTCT
NR_077060.1:n.453-7_453-5delinsTCT
NM_003002.4:c.315-7_315-5delinsTCT MANE Select NP_002993.1:n.315-7_315-5delinsTCT
NM_001276503.2:c.170-7_170-5delinsTCT NP_001263432.1:n.170-7_170-5delinsTCT
NM_001276504.2:c.198-7_198-5delinsTCT NP_001263433.1:n.198-7_198-5delinsTCT
NM_001276506.2:c.*13-7_*13-5delinsTCT NP_001263435.1:n.*13-7_*13-5delinsTCT
NR_077060.2:n.404-7_404-5delinsTCT