Canonical Allele Identifier: CA343361293

Gene: SDHC

Linked Data

• gnomAD v4: 1-161328481-C-A
• MyVariant Identifiers: chr1:g.161298271C>A (hg19) ; chr1:g.161328481C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161328481C>A , CM000663.2:g.161328481C>A	GRCh38
NC_000001.10:g.161298271C>A , CM000663.1:g.161298271C>A	GRCh37
NC_000001.9:g.159564895C>A	NCBI36
NG_012767.1:g.19106C>A , LRG_317:g.19106C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*164C>A	ENSP00000482902.2:n.*164C>A
ENST00000367975.7:c.163C>A MANE Select	ENSP00000356953.3:p.His55Asn
ENST00000342751.8:c.163C>A	ENSP00000356952.3:p.His55Asn
ENST00000367975.6:c.163C>A	ENSP00000356953.2:p.His55Asn
ENST00000392169.6:c.21-12113C>A	ENSP00000376009.2:n.21-12113C>A
ENST00000432287.6:c.77+4811C>A	ENSP00000390558.2:n.77+4811C>A
ENST00000470743.4:c.261C>A
ENST00000504963.5:c.163C>A	ENSP00000423929.1:p.His55Asn
ENST00000513009.5:c.77+4811C>A	ENSP00000423260.1:n.77+4811C>A
ENST00000515731.1:n.637C>A
NM_001035511.1:c.163C>A	NP_001030588.1:p.His55Asn
NM_001035512.1:c.77+4811C>A	NP_001030589.1:n.77+4811C>A
NM_001035513.1:c.21-12113C>A	NP_001030590.1:n.21-12113C>A
NM_001278172.1:c.77+4811C>A	NP_001265101.1:n.77+4811C>A
NM_003001.3:c.163C>A , LRG_317t1:c.163C>A	NP_002992.1:p.His55Asn
NR_103459.1:n.193C>A
NM_001035511.2:c.163C>A	NP_001030588.1:p.His55Asn
NM_001035512.2:c.77+4811C>A	NP_001030589.1:n.77+4811C>A
NM_001035513.2:c.21-12113C>A	NP_001030590.1:n.21-12113C>A
NM_001278172.2:c.77+4811C>A	NP_001265101.1:n.77+4811C>A
NM_003001.5:c.163C>A MANE Select	NP_002992.1:p.His55Asn
NR_103459.2:n.188C>A