Canonical Allele Identifier: CA421501104

Gene: SDHC

Linked Data

• ClinVar Variation Id: 486429
• ClinVar RCV Id: RCV000573492 ; RCV001468401
• dbSNP Id: rs1553265821
• MyVariant Identifiers: chr1:g.161326609C>T (hg19) ; chr1:g.161356819C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161356819C>T , CM000663.2:g.161356819C>T	GRCh38
NC_000001.10:g.161326609C>T , CM000663.1:g.161326609C>T	GRCh37
NC_000001.9:g.159593233C>T	NCBI36
NG_012767.1:g.47444C>T , LRG_317:g.47444C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000470743.5:c.*385C>T	ENSP00000482902.2:n.*385C>T
ENST00000367975.7:c.384C>T MANE Select	ENSP00000356953.3:p.Thr128=
ENST00000342751.8:c.242-5510C>T	ENSP00000356952.3:n.242-5510C>T
ENST00000367975.6:c.384C>T	ENSP00000356953.2:p.Thr128=
ENST00000392169.6:c.225C>T	ENSP00000376009.2:p.Thr75=
ENST00000432287.6:c.282C>T	ENSP00000390558.2:p.Thr94=
ENST00000470743.4:c.482C>T
ENST00000504963.5:c.*207C>T	ENSP00000423929.1:n.*207C>T
ENST00000513009.5:c.140-5510C>T	ENSP00000423260.1:n.140-5510C>T
NM_001035511.1:c.242-5510C>T	NP_001030588.1:n.242-5510C>T
NM_001035512.1:c.282C>T	NP_001030589.1:p.Thr94=
NM_001035513.1:c.225C>T	NP_001030590.1:p.Thr75=
NM_001278172.1:c.140-5510C>T	NP_001265101.1:n.140-5510C>T
NM_003001.3:c.384C>T , LRG_317t1:c.384C>T	NP_002992.1:p.Thr128=
NR_103459.1:n.441C>T
NM_001035511.2:c.242-5510C>T	NP_001030588.1:n.242-5510C>T
NM_001035512.2:c.282C>T	NP_001030589.1:p.Thr94=
NM_001035513.2:c.225C>T	NP_001030590.1:p.Thr75=
NM_001278172.2:c.140-5510C>T	NP_001265101.1:n.140-5510C>T
NM_003001.5:c.384C>T MANE Select	NP_002992.1:p.Thr128=
NR_103459.2:n.436C>T