Canonical Allele Identifier: CA421501068

Gene: SDHC

Linked Data

• COSMIC: COSM5812462 ; COSM5812463
• MyVariant Identifiers: chr1:g.161326570A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161356780A>T , CM000663.2:g.161356780A>T	GRCh38
NC_000001.10:g.161326570A>T , CM000663.1:g.161326570A>T	GRCh37
NC_000001.9:g.159593194A>T	NCBI36
NG_012767.1:g.47405A>T , LRG_317:g.47405A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*346A>T	ENSP00000482902.2:n.*346A>T
ENST00000367975.7:c.345A>T MANE Select	ENSP00000356953.3:p.Thr115=
ENST00000342751.8:c.242-5549A>T	ENSP00000356952.3:n.242-5549A>T
ENST00000367975.6:c.345A>T	ENSP00000356953.2:p.Thr115=
ENST00000392169.6:c.186A>T	ENSP00000376009.2:p.Thr62=
ENST00000432287.6:c.243A>T	ENSP00000390558.2:p.Thr81=
ENST00000470743.4:c.443A>T
ENST00000504963.5:c.*168A>T	ENSP00000423929.1:n.*168A>T
ENST00000513009.5:c.140-5549A>T	ENSP00000423260.1:n.140-5549A>T
NM_001035511.1:c.242-5549A>T	NP_001030588.1:n.242-5549A>T
NM_001035512.1:c.243A>T	NP_001030589.1:p.Thr81=
NM_001035513.1:c.186A>T	NP_001030590.1:p.Thr62=
NM_001278172.1:c.140-5549A>T	NP_001265101.1:n.140-5549A>T
NM_003001.3:c.345A>T , LRG_317t1:c.345A>T	NP_002992.1:p.Thr115=
NR_103459.1:n.402A>T
NM_001035511.2:c.242-5549A>T	NP_001030588.1:n.242-5549A>T
NM_001035512.2:c.243A>T	NP_001030589.1:p.Thr81=
NM_001035513.2:c.186A>T	NP_001030590.1:p.Thr62=
NM_001278172.2:c.140-5549A>T	NP_001265101.1:n.140-5549A>T
NM_003001.5:c.345A>T MANE Select	NP_002992.1:p.Thr115=
NR_103459.2:n.397A>T