Canonical Allele Identifier: CA382618725
Gene: SDHD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112094806G>C , CM000673.2:g.112094806G>C GRCh38
NC_000011.9:g.111965530G>C , CM000673.1:g.111965530G>C GRCh37
NC_000011.8:g.111470740G>C NCBI36
NG_012337.2:g.12960G>C
NG_012337.3:g.12960G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.*55G>C ENSP00000432946.2:n.*55G>C
ENST00000534010.2:c.314+5795G>C ENSP00000433202.2:n.314+5795G>C
ENST00000375549.8:c.316G>C MANE Select ENSP00000364699.3:p.Gly106Arg
ENST00000528021.6:c.314+5795G>C ENSP00000432465.1:n.314+5795G>C
ENST00000375549.7:c.316G>C ENSP00000364699.3:p.Gly106Arg
ENST00000525291.5:c.199G>C ENSP00000436669.1:p.Gly67Arg
ENST00000525987.5:n.319+5795G>C
ENST00000526592.5:c.*14G>C ENSP00000432005.1:n.*14G>C
ENST00000528021.5:c.314+5795G>C ENSP00000432465.1:n.314+5795G>C
ENST00000528048.5:c.171G>C ENSP00000436217.1:p.Trp57Cys
ENST00000528182.5:c.309G>C ENSP00000435475.1:p.Gly103=
ENST00000530923.5:c.360G>C
ENST00000531744.5:c.314+5795G>C ENSP00000456957.1:n.314+5795G>C
ENST00000532699.1:c.314+5795G>C ENSP00000456434.1:n.314+5795G>C
ENST00000534010.1:c.145+5795G>C
NM_001276503.1:c.171G>C NP_001263432.1:p.Trp57Cys
NM_001276504.1:c.199G>C NP_001263433.1:p.Gly67Arg
NM_001276506.1:c.*14G>C NP_001263435.1:n.*14G>C
NM_003002.3:c.316G>C NP_002993.1:p.Gly106Arg
NR_077060.1:n.454G>C
NM_003002.4:c.316G>C MANE Select NP_002993.1:p.Gly106Arg
NM_001276503.2:c.171G>C NP_001263432.1:p.Trp57Cys
NM_001276504.2:c.199G>C NP_001263433.1:p.Gly67Arg
NM_001276506.2:c.*14G>C NP_001263435.1:n.*14G>C
NR_077060.2:n.405G>C