Canonical Allele Identifier: CA343456722

Gene: SDHC

Linked Data

• ClinVar Variation Id: 1735970
• ClinVar RCV Id: RCV002357443
• MyVariant Identifiers: chr1:g.161326614A>G (hg19) ; chr1:g.161356824A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161356824A>G , CM000663.2:g.161356824A>G	GRCh38
NC_000001.10:g.161326614A>G , CM000663.1:g.161326614A>G	GRCh37
NC_000001.9:g.159593238A>G	NCBI36
NG_012767.1:g.47449A>G , LRG_317:g.47449A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000470743.5:c.*390A>G	ENSP00000482902.2:n.*390A>G
ENST00000367975.7:c.389A>G MANE Select	ENSP00000356953.3:p.Asn130Ser
ENST00000342751.8:c.242-5505A>G	ENSP00000356952.3:n.242-5505A>G
ENST00000367975.6:c.389A>G	ENSP00000356953.2:p.Asn130Ser
ENST00000392169.6:c.230A>G	ENSP00000376009.2:p.Asn77Ser
ENST00000432287.6:c.287A>G	ENSP00000390558.2:p.Asn96Ser
ENST00000470743.4:c.487A>G
ENST00000504963.5:c.*212A>G	ENSP00000423929.1:n.*212A>G
ENST00000513009.5:c.140-5505A>G	ENSP00000423260.1:n.140-5505A>G
NM_001035511.1:c.242-5505A>G	NP_001030588.1:n.242-5505A>G
NM_001035512.1:c.287A>G	NP_001030589.1:p.Asn96Ser
NM_001035513.1:c.230A>G	NP_001030590.1:p.Asn77Ser
NM_001278172.1:c.140-5505A>G	NP_001265101.1:n.140-5505A>G
NM_003001.3:c.389A>G , LRG_317t1:c.389A>G	NP_002992.1:p.Asn130Ser
NR_103459.1:n.446A>G
NM_001035511.2:c.242-5505A>G	NP_001030588.1:n.242-5505A>G
NM_001035512.2:c.287A>G	NP_001030589.1:p.Asn96Ser
NM_001035513.2:c.230A>G	NP_001030590.1:p.Asn77Ser
NM_001278172.2:c.140-5505A>G	NP_001265101.1:n.140-5505A>G
NM_003001.5:c.389A>G MANE Select	NP_002992.1:p.Asn130Ser
NR_103459.2:n.441A>G