Canonical Allele Identifier: CA891843045

Gene: SDHC

Linked Data

• ClinVar Variation Id: 570507
• ClinVar RCV Id: RCV000691372
• dbSNP Id: rs1558182956
• MyVariant Identifiers: chr1:g.161326631del (hg19) ; chr1:g.161356841del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161356841del , CM000663.2:g.161356841del	GRCh38
NC_000001.10:g.161326631del , CM000663.1:g.161326631del	GRCh37
NC_000001.9:g.159593255del	NCBI36
NG_012767.1:g.47466del , LRG_317:g.47466del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*406+1del
ENST00000367975.7:c.405+1del
ENST00000342751.8:c.242-5488del	ENSP00000356952.3:n.242-5488del
ENST00000367975.6:c.405+1del
ENST00000392169.6:c.246+1del
ENST00000432287.6:c.303+1del
ENST00000470743.4:c.503+1del
ENST00000504963.5:c.*228+1del
ENST00000513009.5:c.140-5488del	ENSP00000423260.1:n.140-5488del
NM_001035511.1:c.242-5488del	NP_001030588.1:n.242-5488del
NM_001035512.1:c.303+1del
NM_001035513.1:c.246+1del
NM_001278172.1:c.140-5488del	NP_001265101.1:n.140-5488del
NM_003001.3:c.405+1del , LRG_317t1:c.405+1del
NR_103459.1:n.462+1del
NM_001035511.2:c.242-5488del	NP_001030588.1:n.242-5488del
NM_001035512.2:c.303+1del
NM_001035513.2:c.246+1del
NM_001278172.2:c.140-5488del	NP_001265101.1:n.140-5488del
NM_003001.5:c.405+1del
NR_103459.2:n.457+1del