Canonical Allele Identifier: CA343365994

Gene: SDHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161340635C>T , CM000663.2:g.161340635C>T	GRCh38
NC_000001.10:g.161310425C>T , CM000663.1:g.161310425C>T	GRCh37
NC_000001.9:g.159577049C>T	NCBI36
NG_012767.1:g.31260C>T , LRG_317:g.31260C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*222C>T	ENSP00000482902.2:n.*222C>T
ENST00000367975.7:c.221C>T MANE Select	ENSP00000356953.3:p.Thr74Ile
ENST00000342751.8:c.221C>T	ENSP00000356952.3:p.Thr74Ile
ENST00000367975.6:c.221C>T	ENSP00000356953.2:p.Thr74Ile
ENST00000392169.6:c.62C>T	ENSP00000376009.2:p.Thr21Ile
ENST00000432287.6:c.119C>T	ENSP00000390558.2:p.Thr40Ile
ENST00000470743.4:c.319C>T
ENST00000504963.5:c.*44C>T	ENSP00000423929.1:n.*44C>T
ENST00000513009.5:c.119C>T	ENSP00000423260.1:p.Thr40Ile
NM_001035511.1:c.221C>T	NP_001030588.1:p.Thr74Ile
NM_001035512.1:c.119C>T	NP_001030589.1:p.Thr40Ile
NM_001035513.1:c.62C>T	NP_001030590.1:p.Thr21Ile
NM_001278172.1:c.119C>T	NP_001265101.1:p.Thr40Ile
NM_003001.3:c.221C>T , LRG_317t1:c.221C>T	NP_002992.1:p.Thr74Ile
NR_103459.1:n.278C>T
NM_001035511.2:c.221C>T	NP_001030588.1:p.Thr74Ile
NM_001035512.2:c.119C>T	NP_001030589.1:p.Thr40Ile
NM_001035513.2:c.62C>T	NP_001030590.1:p.Thr21Ile
NM_001278172.2:c.119C>T	NP_001265101.1:p.Thr40Ile
NM_003001.5:c.221C>T MANE Select	NP_002992.1:p.Thr74Ile
NR_103459.2:n.273C>T