Canonical Allele Identifier: CA2695215442
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086943dup , CM000673.2:g.112086943dup GRCh38
NC_000011.9:g.111957667dup , CM000673.1:g.111957667dup GRCh37
NC_000011.8:g.111462877dup NCBI36
NG_012337.2:g.5097dup
NG_033145.1:g.4856dup
NG_012337.3:g.5097dup

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.36dup ENSP00000432946.2:p.Ala13CysfsTer?
ENST00000534010.2:c.36dup ENSP00000433202.2:p.Ala13CysfsTer?
ENST00000375549.8:c.36dup MANE Select ENSP00000364699.3:p.Ala13CysfsTer?
ENST00000528021.6:c.36dup ENSP00000432465.1:p.Ala13CysfsTer?
ENST00000640554.1:c.36dup ENSP00000491141.1:p.Ala13CysfsTer?
ENST00000375549.7:c.36dup ENSP00000364699.3:p.Ala13CysfsTer?
ENST00000525291.5:c.36dup ENSP00000436669.1:p.Ala13CysfsTer17
ENST00000525987.5:n.41dup
ENST00000526592.5:c.36dup ENSP00000432005.1:p.Ala13CysfsTer?
ENST00000528021.5:c.36dup ENSP00000432465.1:p.Ala13CysfsTer?
ENST00000528048.5:c.36dup ENSP00000436217.1:p.Ala13CysfsTer?
ENST00000528182.5:c.36dup ENSP00000435475.1:p.Ala13CysfsTer?
ENST00000530923.5:c.26dup
ENST00000531744.5:c.36dup ENSP00000456957.1:p.Ala13CysfsTer?
ENST00000532699.1:c.36dup ENSP00000456434.1:p.Ala13CysfsTer?
ENST00000614349.4:c.36dup ENSP00000480666.1:p.Ala13CysfsTer?
NM_001276503.1:c.36dup NP_001263432.1:p.Ala13CysfsTer?
NM_001276504.1:c.36dup NP_001263433.1:p.Ala13CysfsTer17
NM_001276506.1:c.36dup NP_001263435.1:p.Ala13CysfsTer?
NM_003002.3:c.36dup NP_002993.1:p.Ala13CysfsTer?
NR_077060.1:n.120dup
NM_003002.4:c.36dup MANE Select NP_002993.1:p.Ala13CysfsTer?
NM_001276503.2:c.36dup NP_001263432.1:p.Ala13CysfsTer?
NM_001276504.2:c.36dup NP_001263433.1:p.Ala13CysfsTer17
NM_001276506.2:c.36dup NP_001263435.1:p.Ala13CysfsTer?
NR_077060.2:n.71dup