Canonical Allele Identifier: CA2000553583
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112094713A= , CM000673.2:g.112094713A= GRCh38
NC_000011.9:g.111965437A= , CM000673.1:g.111965437A= GRCh37
NC_000011.8:g.111470647A= NCBI36
NG_012337.2:g.12867A=
NG_012337.3:g.12867A=

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.*54-92A= ENSP00000432946.2:n.*54-92A=
ENST00000534010.2:c.314+5702A= ENSP00000433202.2:n.314+5702A=
ENST00000375549.8:c.315-92A= MANE Select ENSP00000364699.3:n.315-92A=
ENST00000528021.6:c.314+5702A= ENSP00000432465.1:n.314+5702A=
ENST00000375549.7:c.315-92A= ENSP00000364699.3:n.315-92A=
ENST00000525291.5:c.198-92A= ENSP00000436669.1:n.198-92A=
ENST00000525987.5:n.319+5702A=
ENST00000526592.5:c.*13-92A= ENSP00000432005.1:n.*13-92A=
ENST00000528021.5:c.314+5702A= ENSP00000432465.1:n.314+5702A=
ENST00000528048.5:c.170-92A= ENSP00000436217.1:n.170-92A=
ENST00000528182.5:c.308-92A= ENSP00000435475.1:n.308-92A=
ENST00000530923.5:c.359-92A=
ENST00000531744.5:c.314+5702A= ENSP00000456957.1:n.314+5702A=
ENST00000532699.1:c.314+5702A= ENSP00000456434.1:n.314+5702A=
ENST00000534010.1:c.145+5702A=
NM_001276503.1:c.170-92A= NP_001263432.1:n.170-92A=
NM_001276504.1:c.198-92A= NP_001263433.1:n.198-92A=
NM_001276506.1:c.*13-92A= NP_001263435.1:n.*13-92A=
NM_003002.3:c.315-92A= NP_002993.1:n.315-92A=
NR_077060.1:n.453-92A=
NM_003002.4:c.315-92A= MANE Select NP_002993.1:n.315-92A=
NM_001276503.2:c.170-92A= NP_001263432.1:n.170-92A=
NM_001276504.2:c.198-92A= NP_001263433.1:n.198-92A=
NM_001276506.2:c.*13-92A= NP_001263435.1:n.*13-92A=
NR_077060.2:n.404-92A=