Canonical Allele Identifier: CA343361210

Gene: SDHC

Linked Data

• ClinVar Variation Id: 1773114
• ClinVar RCV Id: RCV002394770 ; RCV004007321
• MyVariant Identifiers: chr1:g.161298253A>G (hg19) ; chr1:g.161328463A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161328463A>G , CM000663.2:g.161328463A>G	GRCh38
NC_000001.10:g.161298253A>G , CM000663.1:g.161298253A>G	GRCh37
NC_000001.9:g.159564877A>G	NCBI36
NG_012767.1:g.19088A>G , LRG_317:g.19088A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*146A>G	ENSP00000482902.2:n.*146A>G
ENST00000367975.7:c.145A>G MANE Select	ENSP00000356953.3:p.Asn49Asp
ENST00000342751.8:c.145A>G	ENSP00000356952.3:p.Asn49Asp
ENST00000367975.6:c.145A>G	ENSP00000356953.2:p.Asn49Asp
ENST00000392169.6:c.21-12131A>G	ENSP00000376009.2:n.21-12131A>G
ENST00000432287.6:c.77+4793A>G	ENSP00000390558.2:n.77+4793A>G
ENST00000470743.4:c.243A>G
ENST00000504963.5:c.145A>G	ENSP00000423929.1:p.Asn49Asp
ENST00000513009.5:c.77+4793A>G	ENSP00000423260.1:n.77+4793A>G
ENST00000515731.1:n.619A>G
NM_001035511.1:c.145A>G	NP_001030588.1:p.Asn49Asp
NM_001035512.1:c.77+4793A>G	NP_001030589.1:n.77+4793A>G
NM_001035513.1:c.21-12131A>G	NP_001030590.1:n.21-12131A>G
NM_001278172.1:c.77+4793A>G	NP_001265101.1:n.77+4793A>G
NM_003001.3:c.145A>G , LRG_317t1:c.145A>G	NP_002992.1:p.Asn49Asp
NR_103459.1:n.175A>G
NM_001035511.2:c.145A>G	NP_001030588.1:p.Asn49Asp
NM_001035512.2:c.77+4793A>G	NP_001030589.1:n.77+4793A>G
NM_001035513.2:c.21-12131A>G	NP_001030590.1:n.21-12131A>G
NM_001278172.2:c.77+4793A>G	NP_001265101.1:n.77+4793A>G
NM_003001.5:c.145A>G MANE Select	NP_002992.1:p.Asn49Asp
NR_103459.2:n.170A>G