Canonical Allele Identifier: CA343359474

Gene: SDHC

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161323644C>A , CM000663.2:g.161323644C>A	GRCh38
NC_000001.10:g.161293434C>A , CM000663.1:g.161293434C>A	GRCh37
NC_000001.9:g.159560058C>A	NCBI36
NG_012767.1:g.14269C>A , LRG_317:g.14269C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.51C>A	ENSP00000482902.2:p.His17Gln
ENST00000367975.7:c.51C>A MANE Select	ENSP00000356953.3:p.His17Gln
ENST00000342751.8:c.51C>A	ENSP00000356952.3:p.His17Gln
ENST00000367975.6:c.51C>A	ENSP00000356953.2:p.His17Gln
ENST00000392169.6:c.20+9219C>A	ENSP00000376009.2:n.20+9219C>A
ENST00000432287.6:c.51C>A	ENSP00000390558.2:p.His17Gln
ENST00000470743.4:c.31C>A
ENST00000504963.5:c.51C>A	ENSP00000423929.1:p.His17Gln
ENST00000513009.5:c.51C>A	ENSP00000423260.1:p.His17Gln
ENST00000515731.1:n.525C>A
NM_001035511.1:c.51C>A	NP_001030588.1:p.His17Gln
NM_001035512.1:c.51C>A	NP_001030589.1:p.His17Gln
NM_001035513.1:c.20+9219C>A	NP_001030590.1:n.20+9219C>A
NM_001278172.1:c.51C>A	NP_001265101.1:p.His17Gln
NM_003001.3:c.51C>A , LRG_317t1:c.51C>A	NP_002992.1:p.His17Gln
NR_103459.1:n.81C>A
NM_001035511.2:c.51C>A	NP_001030588.1:p.His17Gln
NM_001035512.2:c.51C>A	NP_001030589.1:p.His17Gln
NM_001035513.2:c.20+9219C>A	NP_001030590.1:n.20+9219C>A
NM_001278172.2:c.51C>A	NP_001265101.1:p.His17Gln
NM_003001.5:c.51C>A MANE Select	NP_002992.1:p.His17Gln
NR_103459.2:n.76C>A