Canonical Allele Identifier: CA2000553954
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112094864A= , CM000673.2:g.112094864A= GRCh38
NC_000011.9:g.111965588A= , CM000673.1:g.111965588A= GRCh37
NC_000011.8:g.111470798A= NCBI36
NG_012337.2:g.13018A=
NG_012337.3:g.13018A=

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.*113A= ENSP00000432946.2:n.*113A=
ENST00000534010.2:c.314+5853A= ENSP00000433202.2:n.314+5853A=
ENST00000375549.8:c.374A= MANE Select ENSP00000364699.3:p.Lys125=
ENST00000528021.6:c.314+5853A= ENSP00000432465.1:n.314+5853A=
ENST00000375549.7:c.374A= ENSP00000364699.3:p.Lys125=
ENST00000525291.5:c.257A= ENSP00000436669.1:p.Lys86=
ENST00000525987.5:n.319+5853A=
ENST00000526592.5:c.*72A= ENSP00000432005.1:n.*72A=
ENST00000528021.5:c.314+5853A= ENSP00000432465.1:n.314+5853A=
ENST00000528048.5:c.229A= ENSP00000436217.1:p.Arg77=
ENST00000528182.5:c.367A= ENSP00000435475.1:p.Arg123=
ENST00000530923.5:c.418A=
ENST00000531744.5:c.314+5853A= ENSP00000456957.1:n.314+5853A=
ENST00000532699.1:c.314+5853A= ENSP00000456434.1:n.314+5853A=
ENST00000534010.1:c.145+5853A=
NM_001276503.1:c.229A= NP_001263432.1:p.Arg77=
NM_001276504.1:c.257A= NP_001263433.1:p.Lys86=
NM_001276506.1:c.*72A= NP_001263435.1:n.*72A=
NM_003002.3:c.374A= NP_002993.1:p.Lys125=
NR_077060.1:n.512A=
NM_003002.4:c.374A= MANE Select NP_002993.1:p.Lys125=
NM_001276503.2:c.229A= NP_001263432.1:p.Arg77=
NM_001276504.2:c.257A= NP_001263433.1:p.Lys86=
NM_001276506.2:c.*72A= NP_001263435.1:n.*72A=
NR_077060.2:n.463A=