Canonical Allele Identifier: CA421501048
Gene: SDHC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.161326543G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161356753G>C , CM000663.2:g.161356753G>C GRCh38
NC_000001.10:g.161326543G>C , CM000663.1:g.161326543G>C GRCh37
NC_000001.9:g.159593167G>C NCBI36
NG_012767.1:g.47378G>C , LRG_317:g.47378G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000470743.5:c.*319G>C ENSP00000482902.2:n.*319G>C
ENST00000367975.7:c.318G>C MANE Select ENSP00000356953.3:p.Leu106=
ENST00000342751.8:c.242-5576G>C ENSP00000356952.3:n.242-5576G>C
ENST00000367975.6:c.318G>C ENSP00000356953.2:p.Leu106=
ENST00000392169.6:c.159G>C ENSP00000376009.2:p.Leu53=
ENST00000432287.6:c.216G>C ENSP00000390558.2:p.Leu72=
ENST00000470743.4:c.416G>C
ENST00000504963.5:c.*141G>C ENSP00000423929.1:n.*141G>C
ENST00000513009.5:c.140-5576G>C ENSP00000423260.1:n.140-5576G>C
NM_001035511.1:c.242-5576G>C NP_001030588.1:n.242-5576G>C
NM_001035512.1:c.216G>C NP_001030589.1:p.Leu72=
NM_001035513.1:c.159G>C NP_001030590.1:p.Leu53=
NM_001278172.1:c.140-5576G>C NP_001265101.1:n.140-5576G>C
NM_003001.3:c.318G>C , LRG_317t1:c.318G>C NP_002992.1:p.Leu106=
NR_103459.1:n.375G>C
NM_001035511.2:c.242-5576G>C NP_001030588.1:n.242-5576G>C
NM_001035512.2:c.216G>C NP_001030589.1:p.Leu72=
NM_001035513.2:c.159G>C NP_001030590.1:p.Leu53=
NM_001278172.2:c.140-5576G>C NP_001265101.1:n.140-5576G>C
NM_003001.5:c.318G>C MANE Select NP_002992.1:p.Leu106=
NR_103459.2:n.370G>C