Canonical Allele Identifier: CA2580061324

Gene: SDHC

Linked Data

• ClinVar Variation Id: 2030932
• ClinVar RCV Id: RCV002872072

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161356847T>A , CM000663.2:g.161356847T>A	GRCh38
NC_000001.10:g.161326637T>A , CM000663.1:g.161326637T>A	GRCh37
NC_000001.9:g.159593261T>A	NCBI36
NG_012767.1:g.47472T>A , LRG_317:g.47472T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*406+7T>A	ENSP00000482902.2:n.*406+7T>A
ENST00000367975.7:c.405+7T>A MANE Select	ENSP00000356953.3:n.405+7T>A
ENST00000342751.8:c.242-5482T>A	ENSP00000356952.3:n.242-5482T>A
ENST00000367975.6:c.405+7T>A	ENSP00000356953.2:n.405+7T>A
ENST00000392169.6:c.246+7T>A	ENSP00000376009.2:n.246+7T>A
ENST00000432287.6:c.303+7T>A	ENSP00000390558.2:n.303+7T>A
ENST00000470743.4:c.503+7T>A
ENST00000504963.5:c.*228+7T>A	ENSP00000423929.1:n.*228+7T>A
ENST00000513009.5:c.140-5482T>A	ENSP00000423260.1:n.140-5482T>A
NM_001035511.1:c.242-5482T>A	NP_001030588.1:n.242-5482T>A
NM_001035512.1:c.303+7T>A	NP_001030589.1:n.303+7T>A
NM_001035513.1:c.246+7T>A	NP_001030590.1:n.246+7T>A
NM_001278172.1:c.140-5482T>A	NP_001265101.1:n.140-5482T>A
NM_003001.3:c.405+7T>A , LRG_317t1:c.405+7T>A	NP_002992.1:n.405+7T>A
NR_103459.1:n.462+7T>A
NM_001035511.2:c.242-5482T>A	NP_001030588.1:n.242-5482T>A
NM_001035512.2:c.303+7T>A	NP_001030589.1:n.303+7T>A
NM_001035513.2:c.246+7T>A	NP_001030590.1:n.246+7T>A
NM_001278172.2:c.140-5482T>A	NP_001265101.1:n.140-5482T>A
NM_003001.5:c.405+7T>A MANE Select	NP_002992.1:n.405+7T>A
NR_103459.2:n.457+7T>A