Canonical Allele Identifier: CA343457937
Gene: SDHC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161362413A>C , CM000663.2:g.161362413A>C GRCh38
NC_000001.10:g.161332203A>C , CM000663.1:g.161332203A>C GRCh37
NC_000001.9:g.159598827A>C NCBI36
NG_012767.1:g.53038A>C , LRG_317:g.53038A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000470743.5:c.*491A>C ENSP00000482902.2:n.*491A>C
ENST00000367975.7:c.490A>C MANE Select ENSP00000356953.3:p.Met164Leu
ENST00000342751.8:c.326A>C ENSP00000356952.3:p.Tyr109Ser
ENST00000367975.6:c.490A>C ENSP00000356953.2:p.Met164Leu
ENST00000392169.6:c.331A>C ENSP00000376009.2:p.Met111Leu
ENST00000432287.6:c.388A>C ENSP00000390558.2:p.Met130Leu
ENST00000470743.4:c.588A>C
ENST00000504963.5:c.*313A>C ENSP00000423929.1:n.*313A>C
ENST00000513009.5:c.224A>C ENSP00000423260.1:p.Tyr75Ser
NM_001035511.1:c.326A>C NP_001030588.1:p.Tyr109Ser
NM_001035512.1:c.388A>C NP_001030589.1:p.Met130Leu
NM_001035513.1:c.331A>C NP_001030590.1:p.Met111Leu
NM_001278172.1:c.224A>C NP_001265101.1:p.Tyr75Ser
NM_003001.3:c.490A>C , LRG_317t1:c.490A>C NP_002992.1:p.Met164Leu
NR_103459.1:n.547A>C
NM_001035511.2:c.326A>C NP_001030588.1:p.Tyr109Ser
NM_001035512.2:c.388A>C NP_001030589.1:p.Met130Leu
NM_001035513.2:c.331A>C NP_001030590.1:p.Met111Leu
NM_001278172.2:c.224A>C NP_001265101.1:p.Tyr75Ser
NM_003001.5:c.490A>C MANE Select NP_002992.1:p.Met164Leu
NR_103459.2:n.542A>C