Canonical Allele Identifier: CA343354980
Gene: SDHC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161314418T>G , CM000663.2:g.161314418T>G GRCh38
NC_000001.10:g.161284208T>G , CM000663.1:g.161284208T>G GRCh37
NC_000001.9:g.159550832T>G NCBI36
NG_008055.1:g.555A>C , LRG_256:g.555A>C
NG_012767.1:g.5043T>G , LRG_317:g.5043T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000470743.5:c.13T>G ENSP00000482902.2:p.Leu5Val
ENST00000367975.7:c.13T>G MANE Select ENSP00000356953.3:p.Leu5Val
ENST00000342751.8:c.13T>G ENSP00000356952.3:p.Leu5Val
ENST00000367975.6:c.13T>G ENSP00000356953.2:p.Leu5Val
ENST00000392169.6:c.13T>G ENSP00000376009.2:p.Leu5Val
ENST00000432287.6:c.13T>G ENSP00000390558.2:p.Leu5Val
ENST00000504963.5:c.13T>G ENSP00000423929.1:p.Leu5Val
ENST00000513009.5:c.13T>G ENSP00000423260.1:p.Leu5Val
ENST00000515731.1:n.38T>G
NM_001035511.1:c.13T>G NP_001030588.1:p.Leu5Val
NM_001035512.1:c.13T>G NP_001030589.1:p.Leu5Val
NM_001035513.1:c.13T>G NP_001030590.1:p.Leu5Val
NM_001278172.1:c.13T>G NP_001265101.1:p.Leu5Val
NM_003001.3:c.13T>G , LRG_317t1:c.13T>G NP_002992.1:p.Leu5Val
NR_103459.1:n.43T>G
NM_001035511.2:c.13T>G NP_001030588.1:p.Leu5Val
NM_001035512.2:c.13T>G NP_001030589.1:p.Leu5Val
NM_001035513.2:c.13T>G NP_001030590.1:p.Leu5Val
NM_001278172.2:c.13T>G NP_001265101.1:p.Leu5Val
NM_003001.5:c.13T>G MANE Select NP_002992.1:p.Leu5Val
NR_103459.2:n.38T>G