Canonical Allele Identifier: CA2000562065
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112088978C= , CM000673.2:g.112088978C= GRCh38
NC_000011.9:g.111959702C= , CM000673.1:g.111959702C= GRCh37
NC_000011.8:g.111464912C= NCBI36
NG_012337.2:g.7132C=
NG_033145.1:g.2821G=
NG_012337.3:g.7132C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000530923.6:c.281C= ENSP00000432946.2:p.Ser94=
ENST00000534010.2:c.281C= ENSP00000433202.2:p.Ser94=
ENST00000375549.8:c.281C= MANE Select ENSP00000364699.3:p.Ser94=
ENST00000528021.6:c.281C= ENSP00000432465.1:p.Ser94=
ENST00000640554.1:c.*353C= ENSP00000491141.1:n.*353C=
ENST00000375549.7:c.281C= ENSP00000364699.3:p.Ser94=
ENST00000525291.5:c.164C= ENSP00000436669.1:p.Ser55=
ENST00000525987.5:n.286C=
ENST00000526592.5:c.281C= ENSP00000432005.1:p.Ser94=
ENST00000528021.5:c.281C= ENSP00000432465.1:p.Ser94=
ENST00000528048.5:c.169+1005C= ENSP00000436217.1:n.169+1005C=
ENST00000528182.5:c.281C= ENSP00000435475.1:p.Ser94=
ENST00000530923.5:c.271C=
ENST00000531744.5:c.281C= ENSP00000456957.1:p.Ser94=
ENST00000532699.1:c.281C= ENSP00000456434.1:p.Ser94=
ENST00000534010.1:c.112C=
ENST00000614349.4:c.281C= ENSP00000480666.1:p.Ser94=
NM_001276503.1:c.169+1005C= NP_001263432.1:n.169+1005C=
NM_001276504.1:c.164C= NP_001263433.1:p.Ser55=
NM_001276506.1:c.281C= NP_001263435.1:p.Ser94=
NM_003002.3:c.281C= NP_002993.1:p.Ser94=
NR_077060.1:n.365C=
NM_003002.4:c.281C= MANE Select NP_002993.1:p.Ser94=
NM_001276503.2:c.169+1005C= NP_001263432.1:n.169+1005C=
NM_001276504.2:c.164C= NP_001263433.1:p.Ser55=
NM_001276506.2:c.281C= NP_001263435.1:p.Ser94=
NR_077060.2:n.316C=