Canonical Allele Identifier: CA421501057

Gene: SDHC

Linked Data

• MyVariant Identifiers: chr1:g.161326552G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161356762G>T , CM000663.2:g.161356762G>T	GRCh38
NC_000001.10:g.161326552G>T , CM000663.1:g.161326552G>T	GRCh37
NC_000001.9:g.159593176G>T	NCBI36
NG_012767.1:g.47387G>T , LRG_317:g.47387G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*328G>T	ENSP00000482902.2:n.*328G>T
ENST00000367975.7:c.327G>T MANE Select	ENSP00000356953.3:p.Gly109=
ENST00000342751.8:c.242-5567G>T	ENSP00000356952.3:n.242-5567G>T
ENST00000367975.6:c.327G>T	ENSP00000356953.2:p.Gly109=
ENST00000392169.6:c.168G>T	ENSP00000376009.2:p.Gly56=
ENST00000432287.6:c.225G>T	ENSP00000390558.2:p.Gly75=
ENST00000470743.4:c.425G>T
ENST00000504963.5:c.*150G>T	ENSP00000423929.1:n.*150G>T
ENST00000513009.5:c.140-5567G>T	ENSP00000423260.1:n.140-5567G>T
NM_001035511.1:c.242-5567G>T	NP_001030588.1:n.242-5567G>T
NM_001035512.1:c.225G>T	NP_001030589.1:p.Gly75=
NM_001035513.1:c.168G>T	NP_001030590.1:p.Gly56=
NM_001278172.1:c.140-5567G>T	NP_001265101.1:n.140-5567G>T
NM_003001.3:c.327G>T , LRG_317t1:c.327G>T	NP_002992.1:p.Gly109=
NR_103459.1:n.384G>T
NM_001035511.2:c.242-5567G>T	NP_001030588.1:n.242-5567G>T
NM_001035512.2:c.225G>T	NP_001030589.1:p.Gly75=
NM_001035513.2:c.168G>T	NP_001030590.1:p.Gly56=
NM_001278172.2:c.140-5567G>T	NP_001265101.1:n.140-5567G>T
NM_003001.5:c.327G>T MANE Select	NP_002992.1:p.Gly109=
NR_103459.2:n.379G>T