Canonical Allele Identifier: CA2574979448
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112094747dup , CM000673.2:g.112094747dup GRCh38
NC_000011.9:g.111965471dup , CM000673.1:g.111965471dup GRCh37
NC_000011.8:g.111470681dup NCBI36
NG_012337.2:g.12901dup
NG_012337.3:g.12901dup

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.*54-58dup ENSP00000432946.2:n.*54-58dup
ENST00000534010.2:c.314+5736dup ENSP00000433202.2:n.314+5736dup
ENST00000375549.8:c.315-58dup MANE Select ENSP00000364699.3:n.315-58dup
ENST00000528021.6:c.314+5736dup ENSP00000432465.1:n.314+5736dup
ENST00000375549.7:c.315-58dup ENSP00000364699.3:n.315-58dup
ENST00000525291.5:c.198-58dup ENSP00000436669.1:n.198-58dup
ENST00000525987.5:n.319+5736dup
ENST00000526592.5:c.*13-58dup ENSP00000432005.1:n.*13-58dup
ENST00000528021.5:c.314+5736dup ENSP00000432465.1:n.314+5736dup
ENST00000528048.5:c.170-58dup ENSP00000436217.1:n.170-58dup
ENST00000528182.5:c.308-58dup ENSP00000435475.1:n.308-58dup
ENST00000530923.5:c.359-58dup
ENST00000531744.5:c.314+5736dup ENSP00000456957.1:n.314+5736dup
ENST00000532699.1:c.314+5736dup ENSP00000456434.1:n.314+5736dup
ENST00000534010.1:c.145+5736dup
NM_001276503.1:c.170-58dup NP_001263432.1:n.170-58dup
NM_001276504.1:c.198-58dup NP_001263433.1:n.198-58dup
NM_001276506.1:c.*13-58dup NP_001263435.1:n.*13-58dup
NM_003002.3:c.315-58dup NP_002993.1:n.315-58dup
NR_077060.1:n.453-58dup
NM_003002.4:c.315-58dup MANE Select NP_002993.1:n.315-58dup
NM_001276503.2:c.170-58dup NP_001263432.1:n.170-58dup
NM_001276504.2:c.198-58dup NP_001263433.1:n.198-58dup
NM_001276506.2:c.*13-58dup NP_001263435.1:n.*13-58dup
NR_077060.2:n.404-58dup