Canonical Allele Identifier: CA343361108

Gene: SDHC

Linked Data

• ClinVar Variation Id: 1769052
• ClinVar RCV Id: RCV002383269
• MyVariant Identifiers: chr1:g.161298236A>T (hg19) ; chr1:g.161328446A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161328446A>T , CM000663.2:g.161328446A>T	GRCh38
NC_000001.10:g.161298236A>T , CM000663.1:g.161298236A>T	GRCh37
NC_000001.9:g.159564860A>T	NCBI36
NG_012767.1:g.19071A>T , LRG_317:g.19071A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*129A>T	ENSP00000482902.2:n.*129A>T
ENST00000367975.7:c.128A>T MANE Select	ENSP00000356953.3:p.Asn43Ile
ENST00000342751.8:c.128A>T	ENSP00000356952.3:p.Asn43Ile
ENST00000367975.6:c.128A>T	ENSP00000356953.2:p.Asn43Ile
ENST00000392169.6:c.21-12148A>T	ENSP00000376009.2:n.21-12148A>T
ENST00000432287.6:c.77+4776A>T	ENSP00000390558.2:n.77+4776A>T
ENST00000470743.4:c.226A>T
ENST00000504963.5:c.128A>T	ENSP00000423929.1:p.Asn43Ile
ENST00000513009.5:c.77+4776A>T	ENSP00000423260.1:n.77+4776A>T
ENST00000515731.1:n.602A>T
NM_001035511.1:c.128A>T	NP_001030588.1:p.Asn43Ile
NM_001035512.1:c.77+4776A>T	NP_001030589.1:n.77+4776A>T
NM_001035513.1:c.21-12148A>T	NP_001030590.1:n.21-12148A>T
NM_001278172.1:c.77+4776A>T	NP_001265101.1:n.77+4776A>T
NM_003001.3:c.128A>T , LRG_317t1:c.128A>T	NP_002992.1:p.Asn43Ile
NR_103459.1:n.158A>T
NM_001035511.2:c.128A>T	NP_001030588.1:p.Asn43Ile
NM_001035512.2:c.77+4776A>T	NP_001030589.1:n.77+4776A>T
NM_001035513.2:c.21-12148A>T	NP_001030590.1:n.21-12148A>T
NM_001278172.2:c.77+4776A>T	NP_001265101.1:n.77+4776A>T
NM_003001.5:c.128A>T MANE Select	NP_002992.1:p.Asn43Ile
NR_103459.2:n.153A>T