Canonical Allele Identifier: CA046289

Gene: SDHC

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161314406A>G , CM000663.2:g.161314406A>G	GRCh38
NC_000001.10:g.161284196A>G , CM000663.1:g.161284196A>G	GRCh37
NC_000001.9:g.159550820A>G	NCBI36
NG_008055.1:g.567T>C , LRG_256:g.567T>C
NG_012767.1:g.5031A>G , LRG_317:g.5031A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.1A>G	ENSP00000482902.2:p.Met1Val
ENST00000367975.7:c.1A>G MANE Select	ENSP00000356953.3:p.Met1Val
ENST00000342751.8:c.1A>G	ENSP00000356952.3:p.Met1Val
ENST00000367975.6:c.1A>G	ENSP00000356953.2:p.Met1Val
ENST00000392169.6:c.1A>G	ENSP00000376009.2:p.Met1Val
ENST00000432287.6:c.1A>G	ENSP00000390558.2:p.Met1Val
ENST00000504963.5:c.1A>G	ENSP00000423929.1:p.Met1Val
ENST00000513009.5:c.1A>G	ENSP00000423260.1:p.Met1Val
ENST00000515731.1:n.26A>G
NM_001035511.1:c.1A>G	NP_001030588.1:p.Met1Val
NM_001035512.1:c.1A>G	NP_001030589.1:p.Met1Val
NM_001035513.1:c.1A>G	NP_001030590.1:p.Met1Val
NM_001278172.1:c.1A>G	NP_001265101.1:p.Met1Val
NM_003001.3:c.1A>G , LRG_317t1:c.1A>G	NP_002992.1:p.Met1Val
NR_103459.1:n.31A>G
NM_001035511.2:c.1A>G	NP_001030588.1:p.Met1Val
NM_001035512.2:c.1A>G	NP_001030589.1:p.Met1Val
NM_001035513.2:c.1A>G	NP_001030590.1:p.Met1Val
NM_001278172.2:c.1A>G	NP_001265101.1:p.Met1Val
NM_003001.5:c.1A>G MANE Select	NP_002992.1:p.Met1Val
NR_103459.2:n.26A>G