Canonical Allele Identifier: CA343456599

Gene: SDHC

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161356790G>A , CM000663.2:g.161356790G>A	GRCh38
NC_000001.10:g.161326580G>A , CM000663.1:g.161326580G>A	GRCh37
NC_000001.9:g.159593204G>A	NCBI36
NG_012767.1:g.47415G>A , LRG_317:g.47415G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*356G>A	ENSP00000482902.2:n.*356G>A
ENST00000367975.7:c.355G>A MANE Select	ENSP00000356953.3:p.Ala119Thr
ENST00000342751.8:c.242-5539G>A	ENSP00000356952.3:n.242-5539G>A
ENST00000367975.6:c.355G>A	ENSP00000356953.2:p.Ala119Thr
ENST00000392169.6:c.196G>A	ENSP00000376009.2:p.Ala66Thr
ENST00000432287.6:c.253G>A	ENSP00000390558.2:p.Ala85Thr
ENST00000470743.4:c.453G>A
ENST00000504963.5:c.*178G>A	ENSP00000423929.1:n.*178G>A
ENST00000513009.5:c.140-5539G>A	ENSP00000423260.1:n.140-5539G>A
NM_001035511.1:c.242-5539G>A	NP_001030588.1:n.242-5539G>A
NM_001035512.1:c.253G>A	NP_001030589.1:p.Ala85Thr
NM_001035513.1:c.196G>A	NP_001030590.1:p.Ala66Thr
NM_001278172.1:c.140-5539G>A	NP_001265101.1:n.140-5539G>A
NM_003001.3:c.355G>A , LRG_317t1:c.355G>A	NP_002992.1:p.Ala119Thr
NR_103459.1:n.412G>A
NM_001035511.2:c.242-5539G>A	NP_001030588.1:n.242-5539G>A
NM_001035512.2:c.253G>A	NP_001030589.1:p.Ala85Thr
NM_001035513.2:c.196G>A	NP_001030590.1:p.Ala66Thr
NM_001278172.2:c.140-5539G>A	NP_001265101.1:n.140-5539G>A
NM_003001.5:c.355G>A MANE Select	NP_002992.1:p.Ala119Thr
NR_103459.2:n.407G>A